HOOKS #'S 7600,7602,7603,7616
K-Number: K791985 · 1979-10-04
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Device Summary
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.
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
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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