FSH RIA KIT (125I)
FDA 510(k) clearance K772188 · decided 1977-12-22
Clearance details
- K-number
- K772188
- Device name
- FSH RIA KIT (125I)
- Applicant
- Diagnostic Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 1977-11-25
- Decision date
- 1977-12-22
- Days to decision
- 27 days
- Clearance type
- Traditional
- Product code
- FSH
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| S 4 INSTRUMENT STAND (K884876) | Carl Zeiss, Inc. | 1988-12-15 |
| S 21 INSTRUMENT STAND (K883578) | Carl Zeiss, Inc. | 1988-09-13 |
| STAND, SURG. INSTRUMENT & DRESSING (K821921) | Emerson-Sack-Warner Corp. | 1982-07-30 |
| SKINNY CHIBA NEEDLE & TRAY (K813337) | American Pharmaseal Div. Ahsc | 1982-01-28 |
| BIOPSY NEEDLES & TRAYS (K813338) | American Pharmaseal Div. Ahsc | 1982-01-28 |
| PERCUTANEOUS TRANSHEPATIC CHOLANG. TRAY (K813335) | American Pharmaseal Div. Ahsc | 1982-01-08 |
| MODEL 902 STAND (K780759) | Applied Medical Research | 1978-05-19 |
Recalls involving this device
No recalls on record reference this clearance.