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FDA 510(k)

HILDYARD POST NASAL FORCEP

K-Number: K772377 · 1978-01-17

Decision Date1978-01-17
Product CodeKAE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HILDYARD POST NASAL FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1978-01-17 under 510(k) number K772377. The device is classified under product code KAE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILDYARD POST NASAL FORCEP?

HILDYARD POST NASAL FORCEP is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772377.

When did HILDYARD POST NASAL FORCEP receive FDA 510(k) clearance?

HILDYARD POST NASAL FORCEP received FDA 510(k) clearance on 1978-01-17, under 510(k) number K772377.

Who is the listed applicant for HILDYARD POST NASAL FORCEP?

The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HILDYARD POST NASAL FORCEP?

The FDA product code for HILDYARD POST NASAL FORCEP is KAE.

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 Edward Weck, 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.

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Related Devices (Code: KAE)

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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