Gorman Rupp Industries
Gorman Rupp Industries appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 6, 1977.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K771537 | AQUAMATIC K-MODULE MODEL K-20 | September 6, 1977 |
| K770839 | AQUAMATIC K-77 | June 8, 1977 |
| K770232 | BLOOD/FLUID WARMER MODEL DW-1000A | February 14, 1977 |
| K761337 | AQUAMATIC K-MODULE MODEL K-10 | January 10, 1977 |
| K760910 | DISPOSABLE K-PADS | December 16, 1976 |
| K761087 | ELECTRONIC CONTROL UNIT | December 6, 1976 |