Schmid Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K897140 | THIN CONDOM RAMSES & SHEIK | HIS | 1990-07-13 | View |
| 510(k) | K900679 | MINT SCENTED CONDOMS | HIS | 1990-06-07 | View |
| 510(k) | K884399 | STANDARD LATEX CONDOM | HIS | 1989-03-01 | View |
| 510(k) | K882893 | CONDOMS (RAMSES, SHEIK AND KOROMEX) | HIS | 1988-10-26 | View |
| 510(k) | K880820 | OKAMOTO CONDOMS SPERMICIDALLY LUBRICATED | HIS | 1988-06-21 | View |
| 510(k) | K874791 | CONDOMS (RAMSES EXTRA, SHEIK ELITE AND KOROMEX) | HIS | 1988-04-12 | View |
| 510(k) | K880202 | OKAMOTO CONDOMS | HIS | 1988-02-26 | View |
| 510(k) | K874718 | STANDARD LATEX CONDOMS (RAMSES, SHEIK AND KOROMEX) | HIS | 1987-12-08 | View |
| 510(k) | K822088 | MALE CONDOM | HIS | 1982-11-03 | View |
| 510(k) | K802354 | PROPHYLACTIC W/SPERMICIDAL LUBRICANT | 1980-09-25 | View |
No matching devices.
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