BONE RONGEURS
K-Number: K852993 · 1985-08-07
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Device Summary
Frequently Asked Questions
What is the BONE RONGEURS?
BONE RONGEURS is a medical device that received FDA 510(k) clearance on 1985-08-07. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852993.
When did BONE RONGEURS receive FDA 510(k) clearance?
BONE RONGEURS received FDA 510(k) clearance on 1985-08-07, under 510(k) number K852993.
Who is the listed applicant for BONE RONGEURS?
The FDA 510(k) record lists The Huxley Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
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 The Huxley Instrument Corp. 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.
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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