Company ยท US
John F. Greer Co., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1987. Name variants (Inc, Corp, punctuation) are merged.
5510(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 17, 1987 | K870577 | E-Z LOOP John F. Greer Co., Inc. | EXB |
| Apr 10, 1987 | K870531 | EZ TAC FILTER John F. Greer Co., Inc. | EXB |
| Jan 14, 1987 | K864190 | E-Z HOLD - #4060 John F. Greer Co., Inc. | KMK |
| Dec 4, 1986 | K864189 | ULTRA-GEL - #4083 John F. Greer Co., Inc. | EXB |
| Dec 4, 1986 | K864188 | E-Z HOLD WITH ADHESIVE BASE.-#4065 John F. Greer Co., Inc. | KNX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||