ACU-SYRINGE W/WO NEEDLES
K-Number: K854877 · 1986-02-19
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Device Summary
Frequently Asked Questions
What is the ACU-SYRINGE W/WO NEEDLES?
ACU-SYRINGE W/WO NEEDLES is a medical device that received FDA 510(k) clearance on 1986-02-19. The listed applicant is Acuderm, Inc.. The 510(k) number is K854877.
When did ACU-SYRINGE W/WO NEEDLES receive FDA 510(k) clearance?
ACU-SYRINGE W/WO NEEDLES received FDA 510(k) clearance on 1986-02-19, under 510(k) number K854877.
Who is the listed applicant for ACU-SYRINGE W/WO NEEDLES?
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-SYRINGE W/WO NEEDLES?
The FDA product code for ACU-SYRINGE W/WO NEEDLES is FMF.
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: FMF)
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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