SURGEON'S CHOICE CRUTCH HANDLE
K-Number: K831889 · 1983-07-07
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Device Summary
Frequently Asked Questions
What is the SURGEON'S CHOICE CRUTCH HANDLE?
SURGEON'S CHOICE CRUTCH HANDLE is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is W.K. Wheeler, Inc.. The 510(k) number is K831889.
When did SURGEON'S CHOICE CRUTCH HANDLE receive FDA 510(k) clearance?
SURGEON'S CHOICE CRUTCH HANDLE received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831889.
Who is the listed applicant for SURGEON'S CHOICE CRUTCH HANDLE?
The FDA 510(k) record lists W.K. Wheeler, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGEON'S CHOICE CRUTCH HANDLE?
The FDA product code for SURGEON'S CHOICE CRUTCH HANDLE is INP.
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.
Related Devices (Code: INP)
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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