TSRH H/M HOOK HOLDER
K-Number: K880211 · 1988-03-04
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Device Summary
Frequently Asked Questions
What is the TSRH H/M HOOK HOLDER?
TSRH H/M HOOK HOLDER is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K880211.
When did TSRH H/M HOOK HOLDER receive FDA 510(k) clearance?
TSRH H/M HOOK HOLDER received FDA 510(k) clearance on 1988-03-04, under 510(k) number K880211.
Who is the listed applicant for TSRH H/M HOOK HOLDER?
The FDA 510(k) record lists Warsaw Orthopedic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TSRH H/M HOOK HOLDER?
The FDA product code for TSRH H/M HOOK HOLDER is KWP.
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 Warsaw Orthopedic, 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: KWP)
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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