GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR
K-Number: K952569 · 1996-01-05
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Device Summary
Frequently Asked Questions
What is the GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR?
GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR is a medical device that received FDA 510(k) clearance on 1996-01-05. The listed applicant is Gamp & Assoc.. The 510(k) number is K952569.
When did GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR receive FDA 510(k) clearance?
GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR received FDA 510(k) clearance on 1996-01-05, under 510(k) number K952569.
Who is the listed applicant for GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR?
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 & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR?
The FDA product code for GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR is HQR.
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: HQR)
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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