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FDA 510(k)

GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR

K-Number: K952569 · 1996-01-05

ApplicantGamp & Assoc.
Decision Date1996-01-05
Product CodeHQR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Gamp & Assoc.. It received FDA 510(k) clearance on 1996-01-05 under 510(k) number K952569. The device is classified under product code HQR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 9 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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