UTERINE CURETTE
K-Number: K802313 · 1981-01-12
Advertisement
Device Summary
Frequently Asked Questions
What is the UTERINE CURETTE?
UTERINE CURETTE is a medical device that received FDA 510(k) clearance on 1981-01-12. The listed applicant is Gynemetrics, Inc.. The 510(k) number is K802313.
When did UTERINE CURETTE receive FDA 510(k) clearance?
UTERINE CURETTE received FDA 510(k) clearance on 1981-01-12, under 510(k) number K802313.
Who is the listed applicant for UTERINE CURETTE?
The FDA 510(k) record lists Gynemetrics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UTERINE CURETTE?
The FDA product code for UTERINE CURETTE is HCY.
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 Gynemetrics, 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: HCY)
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.
Advertisement