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FDA 510(k)

THE EMMETT IUD THREAD RETRIEVER

K-Number: K811761 · 1981-09-21

Decision Date1981-09-21
Product CodeHHF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE EMMETT IUD THREAD RETRIEVER is the device name listed in this FDA 510(k) record. The listed applicant is Proto-Med, Inc.. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K811761. The device is classified under product code HHF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE EMMETT IUD THREAD RETRIEVER?

THE EMMETT IUD THREAD RETRIEVER is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is Proto-Med, Inc.. The 510(k) number is K811761.

When did THE EMMETT IUD THREAD RETRIEVER receive FDA 510(k) clearance?

THE EMMETT IUD THREAD RETRIEVER received FDA 510(k) clearance on 1981-09-21, under 510(k) number K811761.

Who is the listed applicant for THE EMMETT IUD THREAD RETRIEVER?

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

What is the FDA product code for THE EMMETT IUD THREAD RETRIEVER?

The FDA product code for THE EMMETT IUD THREAD RETRIEVER is HHF.

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 Proto-Med, 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: HHF)

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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