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FDA 510(k)

ACU-EVAC

K-Number: K930043 · 1994-02-09

ApplicantAcuderm, Inc.
Decision Date1994-02-09
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACU-EVAC is the device name listed in this FDA 510(k) record. The listed applicant is Acuderm, Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K930043. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACU-EVAC?

ACU-EVAC is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Acuderm, Inc.. The 510(k) number is K930043.

When did ACU-EVAC receive FDA 510(k) clearance?

ACU-EVAC received FDA 510(k) clearance on 1994-02-09, under 510(k) number K930043.

Who is the listed applicant for ACU-EVAC?

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-EVAC?

The FDA product code for ACU-EVAC is FYD.

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.

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Related Devices (Code: FYD)

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.

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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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