ACU-CURETTE
K-Number: K891334 · 1989-04-11
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Device Summary
Frequently Asked Questions
What is the ACU-CURETTE?
ACU-CURETTE is a medical device that received FDA 510(k) clearance on 1989-04-11. The listed applicant is Acuderm, Inc.. The 510(k) number is K891334.
When did ACU-CURETTE receive FDA 510(k) clearance?
ACU-CURETTE received FDA 510(k) clearance on 1989-04-11, under 510(k) number K891334.
Who is the listed applicant for ACU-CURETTE?
The FDA 510(k) record lists Acuderm, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACU-CURETTE?
The FDA product code for ACU-CURETTE is FZS.
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 Acuderm, 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: FZS)
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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