GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR— 510(k) K952586

Name: FDA 510(k) clearance K952586
Creator: U.S. Food and Drug Administration
Published: 1995-09-01

Substantially Equivalent

Gamp & Assoc.

FDA 510(k) clearance K952586 for GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR, Substantially Equivalent on 1995-09-01. Applicant: Gamp & Assoc.. Device class: 2.

Clearance details

Applicant: Gamp & Assoc.
Product code: Code MPA
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1995-06-05
Decision date: 1995-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bridgeton, MO, US

Download summary PDF View on FDA.gov ↗

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K952569 — GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR1996-01-05
K952581 — GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTOR1996-01-05
K952585 — GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATOR1996-01-05
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K954307 — GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE1995-12-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.