GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE
K-Number: K954308 · 1995-12-22
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Device Summary
Frequently Asked Questions
What is the GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE?
GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Gamp & Assoc.. The 510(k) number is K954308.
When did GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE receive FDA 510(k) clearance?
GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE received FDA 510(k) clearance on 1995-12-22, under 510(k) number K954308.
Who is the listed applicant for GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE?
The FDA 510(k) record lists Gamp & Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE?
The FDA product code for GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE is HQB.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Gamp & Assoc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HQB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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