FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CRITIKON I.V. FILTER
K Number: K842075
·
Decision Jun 28, 1984
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
51
Review Days
36
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Basic Information
- Device Name
- CRITIKON I.V. FILTER
- K Number
- K842075
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Critikon Company, LLC
- Date Received
- May 23, 1984
- Decision Date
- June 28, 1984
- Product Code
- FPB
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FPB | Filter, Infusion Line | FDA class 2 | General Hospital |
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|---|---|---|---|
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| K992638 | DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400 | Feb 24, 2000 | Substantially Equivalent |
| K982342 | DINAMAP MPS SELECT PORTABLE MONITOR | Aug 14, 1998 | Substantially Equivalent |
| K943709 | DINAMAP PLUS VITAL SIGNS MONOITOR | Jun 16, 1995 | Substantially Equivalent |
| K942700 | DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340 | Mar 1, 1995 | Substantially Equivalent |
| K933404 | CRITIKON CENTRAL STATIN MONITOR | Feb 9, 1994 | Substantially Equivalent |
| K933050 | CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH | Dec 14, 1993 | Substantially Equivalent |
| K915697 | CRITIKON VITAL SIGNS MODULE | Jul 1, 1993 | Substantially Equivalent |
| K921295 | INTRAVENOUS CATHETERS MODIFICATIONS | May 17, 1993 | Substantially Equivalent |