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FDA 510(k)

ACU-SYRINGE W/WO NEEDLES

K-Number: K854877 · 1986-02-19

ApplicantAcuderm, Inc.
Decision Date1986-02-19
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACU-SYRINGE W/WO NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Acuderm, Inc.. It received FDA 510(k) clearance on 1986-02-19 under 510(k) number K854877. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 13 devices →

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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