Company ยท US
Med General
FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1979. Name variants (Inc, Corp, punctuation) are merged.
12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| GDJ | Clamp, Surgical, General & Plastic Surgery | 2 |
| GXY | Electrode, Cutaneous | 2 |
| BXN | Stimulator, Nerve, Battery-Powered | 1 |
| DRT | Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | 1 |
| DXC | Clamp, Vascular | 1 |
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | 1 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 1 |
| IPF | Stimulator, Muscle, Powered | 1 |
| ISB | Stimulator, Muscle, Diagnostic | 1 |
| KDC | Instrument, Surgical, Disposable | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 3, 1979 | K791097 | CEPTORTRODE WITH CEPTOR HESIVE Med General | GXY |
| Jun 22, 1979 | K791098 | SINGLE-USE MINI-BULLDOG Med General | DXC |
| Apr 23, 1979 | K790763 | MAXI-VAC TM Med General | GCY |
| Feb 26, 1979 | K790269 | CEPTOR HESIVE Med General | GXY |
| Dec 15, 1978 | K782006 | MEDGENERAL SINGLE-USE BULLDOG Med General | GDJ |
| Nov 3, 1978 | K781239 | MYO-STIM Med General | IPF |
| Aug 14, 1978 | K780632 | MAXICEPTOR Med General | ISB |
| May 12, 1978 | K780698 | STIMULATORS, NERVE, ELECTRICAL Med General | GZJ |
| Feb 3, 1978 | K780117 | CARDIOMETER Med General | DRT |
| Dec 13, 1977 | K771702 | VESSEL-STABILIZER Med General | KDC |
| Dec 13, 1977 | K771701 | VESSEL-CLUDE Med General | GDJ |
| Sep 30, 1977 | K771765 | MYO-CHECK Med General | BXN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||