Company ยท US
Medical Products Development, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1981. Name variants (Inc, Corp, punctuation) are merged.
13510(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 |
|---|---|---|---|
| Apr 23, 1981 | K810016 | REPLACABLE BATTERY PERFECTEMP CAUTERY Medical Products Development, Inc. | HQP |
| Apr 23, 1981 | K810013 | MULTIPERFECTEMP CAUTERY Medical Products Development, Inc. | HQP |
| Apr 23, 1981 | K810012 | MULTIMICRO SURGICAL CAUTERY Medical Products Development, Inc. | HQP |
| Feb 26, 1981 | K803067 | SURG-FLEX 10 LIGHT Medical Products Development, Inc. | FSQ |
| Feb 12, 1981 | K810015 | MULTIHI-TEMP CAUTERY Medical Products Development, Inc. | HAM |
| Feb 12, 1981 | K810014 | REPLACABLE BATTERY HI-TEMP CAUTERY Medical Products Development, Inc. | HAM |
| Feb 4, 1981 | K802942 | HITEMP. TM 2 LOOPTIP CAUTERY Medical Products Development, Inc. | GEI |
| Jan 23, 1981 | K810019 | SURG-FLEX 15 SURGICAL LIGHT Medical Products Development, Inc. | FSQ |
| Jan 23, 1981 | K810018 | SURG-FLEX 5 SURGICAL LIGHT Medical Products Development, Inc. | FSQ |
| Jan 5, 1981 | K810017 | MICROSURG CAUTERY Medical Products Development, Inc. | HQO |
| Nov 12, 1980 | K802330 | HI-TEMP LOOPTIP SURGICAL CAUTERY Medical Products Development, Inc. | GEI |
| Jun 26, 1980 | K801323 | HI-TEMP SURGICAL CAUTERY Medical Products Development, Inc. | GEI |
| Jun 4, 1980 | K801078 | PERFECTEMP OPHTHALMIC CAUTERY Medical Products Development, Inc. | HQP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||