FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CENTRALYTE BICARBONATE CONCENTRATE
K Number: K821304
·
Decision May 18, 1982
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
122
Applicant Total
43
Review Days
14
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Basic Information
- Device Name
- CENTRALYTE BICARBONATE CONCENTRATE
- K Number
- K821304
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5820
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Erika, Inc.
- Date Received
- May 4, 1982
- Decision Date
- May 18, 1982
- Product Code
- KPO
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- HE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KPO | Dialysate Concentrate For Hemodialysis (Liquid Or Powder) | FDA class 2 | Gastroenterology, Urology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KPO), ordered by most recent decision date.
NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Bicarby Dialysate RFP-404 (RFP-404-W); Bicarby Dialysate RFP-403 (RFP-403-W); Bicarby Dialysate RFP-403 (RFP-403-G); Bicarby Dialysate RFP-453 (RFP-453-W); Bicarby Dialysate RFP-453 (RFP-453-G); Bicarby Dialysate RFP-454 (RFP-454-W); Bicarby Dialysate RFP-454 (RFP-454-G); Bicarby Dialysate RFP-456 (RFP-456-W)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G)
FDA 510(k)
FDA Class 2
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HemoCare Bicarbonate Concentrate Set (BCS)
FDA 510(k)
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pureFLOW 402 (F00012067); pureFLOW 406 (F00012068); pureFLOW 401 (F00012069); pureFLOW 400 (F00012070)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NxStage PureFlow Solution
FDA 510(k)
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Other Clearances by Erika, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K853134 | NATIONAL MED CARE INFUSION PUMP ADM SET #95-0001-8 | Nov 6, 1985 | Substantially Equivalent |
| K852310 | NATURALYTE BICARBONATE CONCENTRATE-DRY PACK | Jul 26, 1985 | Substantially Equivalent |
| K852309 | ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1 | Jul 26, 1985 | Substantially Equivalent |
| K850865 | TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1- | Apr 3, 1985 | Substantially Equivalent |
| K850866 | TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1L | Apr 3, 1985 | Substantially Equivalent |
| K850655 | TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2 | Mar 7, 1985 | Substantially Equivalent |
| K850654 | TORAY INDUS. FILTRYZER HOLLOW FIBER ARTIFICIAL KID | Mar 7, 1985 | Substantially Equivalent |
| K842436 | ERIKA NEGATIVE PRESS. ARTERIAL BLOOD | Jul 13, 1984 | Substantially Equivalent |
| K831175 | FILTRYZER HOLLOW FIBER ARTIF. KIDNEY | Jun 22, 1984 | Substantially Equivalent |
| K831173 | TORAY INDUSTRIES FILTRYZER HOLLOW FIBER | Jun 22, 1984 | Substantially Equivalent |