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FDA 510(k)

MIDDLE EAR PICKS, HOOKS CURETTES,

K-Number: K791120 · 1979-07-10

ApplicantXomed, Inc.
Decision Date1979-07-10
Product CodeGDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIDDLE EAR PICKS, HOOKS CURETTES, is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1979-07-10 under 510(k) number K791120. The device is classified under product code GDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 82 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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