Company ยท US
General Medical Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1993. Name variants (Inc, Corp, punctuation) are merged.
15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| EGJ | Device, Iontophoresis, Other Uses | 2 |
| FRG | Wrap, Sterilization | 2 |
| KMJ | Lubricant, Patient | 2 |
| BSY | Catheters, Suction, Tracheobronchial | 1 |
| BTM | Ventilator, Emergency, Manual (Resuscitator) | 1 |
| EFQ | Gauze/Sponge, Internal | 1 |
| FHX | Jelly, Lubricating, For Transurethral Surgical Instrument | 1 |
| FME | Gown, Examination | 1 |
| FSM | Tray, Surgical, Instrument | 1 |
| FYC | Gown, Isolation, Surgical | 1 |
| KXF | Applicator, Absorbent Tipped, Non-Sterile | 1 |
| LRO | General Surgery Tray | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 27, 1993 | K926269 | PROCEDURE KIT General Medical Co. | LRO |
| Sep 27, 1991 | K912975 | OPERAND LUBRICATING JELLY General Medical Co. | KMJ |
| Aug 7, 1991 | K912132 | OPERAND LUBRICATING JELLY General Medical Co. | FHX |
| Sep 12, 1990 | K903669 | GENESIS INSUFFLATING CATHETER General Medical Co. | BSY |
| May 2, 1990 | K900110 | OPERAND* LUBRICATING JELLY General Medical Co. | KMJ |
| Dec 20, 1985 | K853635 | SUBDERM TM General Medical Co. | EGJ |
| Dec 12, 1984 | K844652 | C.A.S.E. CONTAINER General Medical Co. | FSM |
| Jul 19, 1983 | K831320 | DRIONIC General Medical Co. | EGJ |
| Apr 9, 1982 | K820689 | C.S.R. WRAPPERS General Medical Co. | FRG |
| Mar 18, 1982 | K820521 | STERILIZATION WRAP General Medical Co. | FRG |
| Oct 10, 1980 | K802231 | AIR VIVA II General Medical Co. | BTM |
| Nov 11, 1977 | K772089 | LAPAROTOMY SPOGNE General Medical Co. | EFQ |
| May 26, 1977 | K770583 | MEDI-PAK LEMON GLYCEOIN SWABS General Medical Co. | KXF |
| May 23, 1977 | K770488 | ISOLATION GOWN General Medical Co. | FYC |
| May 6, 1977 | K770476 | EXAM GOWN General Medical Co. | FME |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||