Medical Device Manufacturer · US , Bridgeton , MO

Gamp & Assoc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1995

Total

Cleared

Denied

Gamp & Assoc. has 9 FDA 510(k) cleared medical devices. Based in Bridgeton, US.

Historical record: 9 cleared submissions from 1995 to 1996. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Gamp & Assoc. Filter by specialty or product code using the sidebar.

Gamp & Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gamp & Assoc.

9 devices

1-9 of 9

Cleared Jan 05, 1996

GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR

K952569 · HQR

Ophthalmic · 214d

Cleared Jan 05, 1996

GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTOR

K952581 · MPA

Ophthalmic · 214d

Cleared Jan 05, 1996

GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATOR

K952585 · MPA

Ophthalmic · 214d

Cleared Dec 22, 1995

GAMP & ASSOC. DISPOSABLE ILL ENDOCULAR LASER PROBE

K954306 · HQB

Ophthalmic · 98d

Cleared Dec 22, 1995

GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE

K954307 · HQB

Ophthalmic · 98d

Cleared Dec 22, 1995

GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE

K954308 · HQB

Ophthalmic · 98d

Cleared Sep 01, 1995

GAMP & ASSOCIATES DISPOSABLE BARE END FIBER

K952580 · MPA

Ophthalmic · 88d

Cleared Sep 01, 1995

GAMP & ASSOCIATES DISPOSABLE ENDOILLUMINATOR W/PICK

K952584 · MPA

Ophthalmic · 88d

Cleared Sep 01, 1995

GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR

K952586 · MPA

Ophthalmic · 88d

Gamp & Assoc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gamp & Assoc.

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