FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
UNICAM I
K Number: K770531
·
Decision Apr 5, 1977
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
69
Review Days
15
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Basic Information
- Device Name
- UNICAM I
- K Number
- K770531
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1100
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Union Carbide Corp.
- Date Received
- March 21, 1977
- Decision Date
- April 5, 1977
- Product Code
- IYX
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| IYX | Camera, Scintillation (Gamma) | FDA class 1 | Radiology |
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|---|---|---|---|
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| K812536 | LINDE MARK II | Sep 23, 1981 | Substantially Equivalent |
| K810732 | LINDE MARK II OXYGEN RESERV. TYPE OR-4 | Mar 27, 1981 | Substantially Equivalent |
| K810596 | CENTRIFI CHEM SYSTEM 400 ANALYZER | Mar 17, 1981 | Substantially Equivalent |
| K810129 | CENTRIFICHEM SYSTEM 500 | Feb 2, 1981 | Substantially Equivalent |
| K803216 | CENTRIFICHEM AST/SGOT OPTIMIZED REAGENT | Jan 9, 1981 | Substantially Equivalent |
| K802741 | CENTRIFICHEM COMB. SERUM-BASED CALIB. | Dec 10, 1980 | Substantially Equivalent |
| K802520 | CENTRIFICHEM PIPETTOR ACCURACY CALIB. | Nov 12, 1980 | Substantially Equivalent |