Gelman Instrument Co.
Gelman Instrument Co. appears in FDA public data with 0 recalls, 11 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 3, 1978.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K772078 | RADIAL IMMUNODIFFUSION KIT-HAPTOGLOBIN | February 3, 1978 |
| K772080 | RADIAL IMMUNODIFFUSION KIT-ALPH-L-ANTIT | February 3, 1978 |
| K772074 | RADIAL IMMUNODIFFUSION KIT-TRANSFERRIN | February 3, 1978 |
| K772079 | RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.M | February 3, 1978 |
| K772075 | RADIAL IMMUNODIFFUSION KIT-COMPLEMENT | February 3, 1978 |
| K772073 | RADIAL IMMUNODIFFUSION KIT-COMP. 3 | February 3, 1978 |
| K772076 | RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB. | February 3, 1978 |
| K772077 | RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.G | February 3, 1978 |
| K772325 | DENSITOMETER 18, COMPUTING, AUTO. | January 12, 1978 |
| K771812 | LIPPOPROTEIN ELECTROPHORESIS REAGENT SET | October 18, 1977 |
| K770155 | ALKALINE PHOSPHATASE ISOYZME REAGENT SET | January 31, 1977 |