THE EMMETT IUD THREAD RETRIEVER
K-Number: K811761 · 1981-09-21
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Device Summary
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
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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