Company ยท US
Schmid Laboratories, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1990. Name variants (Inc, Corp, punctuation) are merged.
10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| HIS | Condom | 9 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 13, 1990 | K897140 | THIN CONDOM RAMSES & SHEIK Schmid Laboratories, Inc. | HIS |
| Jun 7, 1990 | K900679 | MINT SCENTED CONDOMS Schmid Laboratories, Inc. | HIS |
| Mar 1, 1989 | K884399 | STANDARD LATEX CONDOM Schmid Laboratories, Inc. | HIS |
| Oct 26, 1988 | K882893 | CONDOMS (RAMSES, SHEIK AND KOROMEX) Schmid Laboratories, Inc. | HIS |
| Jun 21, 1988 | K880820 | OKAMOTO CONDOMS SPERMICIDALLY LUBRICATED Schmid Laboratories, Inc. | HIS |
| Apr 12, 1988 | K874791 | CONDOMS (RAMSES EXTRA, SHEIK ELITE AND KOROMEX) Schmid Laboratories, Inc. | HIS |
| Feb 26, 1988 | K880202 | OKAMOTO CONDOMS Schmid Laboratories, Inc. | HIS |
| Dec 8, 1987 | K874718 | STANDARD LATEX CONDOMS (RAMSES, SHEIK AND KOROMEX) Schmid Laboratories, Inc. | HIS |
| Nov 3, 1982 | K822088 | MALE CONDOM Schmid Laboratories, Inc. | HIS |
| Sep 25, 1980 | K802354 | PROPHYLACTIC W/SPERMICIDAL LUBRICANT Schmid Laboratories, Inc. |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||