CURETTE, UTERINE, VACUUM ASPIRATING
K-Number: K770674 · 1977-04-26
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Device Summary
Frequently Asked Questions
What is the CURETTE, UTERINE, VACUUM ASPIRATING?
CURETTE, UTERINE, VACUUM ASPIRATING is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K770674.
When did CURETTE, UTERINE, VACUUM ASPIRATING receive FDA 510(k) clearance?
CURETTE, UTERINE, VACUUM ASPIRATING received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770674.
Who is the listed applicant for CURETTE, UTERINE, VACUUM ASPIRATING?
The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURETTE, UTERINE, VACUUM ASPIRATING?
The FDA product code for CURETTE, UTERINE, VACUUM ASPIRATING is HHK.
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 American Hospital Supply Corp. 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: HHK)
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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