Company ยท US
Gorman Rupp Industries
FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1977. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 6, 1977 | K771537 | AQUAMATIC K-MODULE MODEL K-20 Gorman Rupp Industries | DWJ |
| Jun 8, 1977 | K770839 | AQUAMATIC K-77 Gorman Rupp Industries | DWJ |
| Feb 14, 1977 | K770232 | BLOOD/FLUID WARMER MODEL DW-1000A Gorman Rupp Industries | BSB |
| Jan 10, 1977 | K761337 | AQUAMATIC K-MODULE MODEL K-10 Gorman Rupp Industries | JRR |
| Dec 16, 1976 | K760910 | DISPOSABLE K-PADS Gorman Rupp Industries | ILO |
| Dec 6, 1976 | K761087 | ELECTRONIC CONTROL UNIT Gorman Rupp Industries | DWJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||