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FDA 510(k)

HOOKS #'S 7600,7602,7603,7616

K-Number: K791985 · 1979-10-04

Decision Date1979-10-04
Product CodeHNQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HOOKS #'S 7600,7602,7603,7616 is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791985. The device is classified under product code HNQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOKS #'S 7600,7602,7603,7616?

HOOKS #'S 7600,7602,7603,7616 is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791985.

When did HOOKS #'S 7600,7602,7603,7616 receive FDA 510(k) clearance?

HOOKS #'S 7600,7602,7603,7616 received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791985.

Who is the listed applicant for HOOKS #'S 7600,7602,7603,7616?

The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOOKS #'S 7600,7602,7603,7616?

The FDA product code for HOOKS #'S 7600,7602,7603,7616 is HNQ.

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 Edward Weck, Inc. 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.

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Related Devices (Code: HNQ)

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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