FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CONTRO I
K Number: K791695
·
Decision Sep 24, 1979
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
52
Review Days
55
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Basic Information
- Device Name
- CONTRO I
- K Number
- K791695
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Hi Chem, Inc.
- Date Received
- July 31, 1979
- Decision Date
- September 24, 1979
- Product Code
- JJY
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JJY | Multi-Analyte Controls, All Kinds (Assayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by Hi Chem, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K960084 | HICHEM GLUCOSE/HK REAGENT KIT | Apr 4, 1996 | Substantially Equivalent |
| K951818 | HICHEM ALT REAGENT KIT | May 15, 1995 | Substantially Equivalent |
| K943684 | HICHEM ENZYME VERIFIER KIT | Oct 4, 1994 | Substantially Equivalent |
| K941764 | HICHEM CALCIUM REAGENT FOR THE SYNCHRON CX3 PROD. NO. 88808 | May 13, 1994 | Substantially Equivalent |
| K902673 | HI CHEM TOTAL PROTEIN/ALBUMIN SERUM RANGE LIN STND | Jul 17, 1990 | Substantially Equivalent |
| K863617 | ION 2/4 FLOW CELL CLEANER (PRODUCT #88656) | Oct 24, 1986 | Substantially Equivalent |
| K862027 | LDP REAGENT CARTRIDGE (NO. 88216) | Jun 13, 1986 | Substantially Equivalent |
| K861893 | GGT REAGENT CARTRIDGE (PRODUCT NO. 88204) | Jun 5, 1986 | Substantially Equivalent |
| K861879 | CK REAGENT CARTRIDGE (PRODUCT NO. 88213) | May 29, 1986 | Substantially Equivalent |
| K861284 | AP REAGENT CARTRIDGE | Apr 28, 1986 | Substantially Equivalent |