Gamp & Assoc.
Bridgeton, MO, US
Gamp & Assoc. appears in FDA device records in Bridgeton, MO. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Gamp & Assoc. between 1995 and 1996. The busiest year on record is 1995, with 6. The most recent is 1996, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1995 | 6 |
| 1996 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K952585 | GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATOR | MPA | Substantially Equivalent | |
| K952581 | GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTOR | MPA | Substantially Equivalent | |
| K952569 | GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR | HQR | Substantially Equivalent | |
| K954308 | GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE | HQB | Substantially Equivalent | |
| K954307 | GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE | HQB | Substantially Equivalent | |
| K954306 | GAMP & ASSOC. DISPOSABLE ILL ENDOCULAR LASER PROBE | HQB | Substantially Equivalent | |
| K952586 | GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR | MPA | Substantially Equivalent | |
| K952584 | GAMP & ASSOCIATES DISPOSABLE ENDOILLUMINATOR W/PICK | MPA | Substantially Equivalent | |
| K952580 | GAMP & ASSOCIATES DISPOSABLE BARE END FIBER | MPA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain