MIDDLE EAR PICKS, HOOKS CURETTES,
K-Number: K791120 · 1979-07-10
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Device Summary
Frequently Asked Questions
What is the MIDDLE EAR PICKS, HOOKS CURETTES,?
MIDDLE EAR PICKS, HOOKS CURETTES, is a medical device that received FDA 510(k) clearance on 1979-07-10. The listed applicant is Xomed, Inc.. The 510(k) number is K791120.
When did MIDDLE EAR PICKS, HOOKS CURETTES, receive FDA 510(k) clearance?
MIDDLE EAR PICKS, HOOKS CURETTES, received FDA 510(k) clearance on 1979-07-10, under 510(k) number K791120.
Who is the listed applicant for MIDDLE EAR PICKS, HOOKS CURETTES,?
The FDA 510(k) record lists Xomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIDDLE EAR PICKS, HOOKS CURETTES,?
The FDA product code for MIDDLE EAR PICKS, HOOKS CURETTES, is GDG.
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 Xomed, 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: GDG)
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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