FDA 510(k)

ACU-PUNCH

K-Number: K831635 · 1983-07-07

Decision Date1983-07-07

Product Code

DecisionSubstantially Equivalent

Device Summary

ACU-PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Acuderm, Inc.. It received FDA 510(k) clearance on 1983-07-07 under 510(k) number K831635. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACU-PUNCH?

ACU-PUNCH is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is Acuderm, Inc.. The 510(k) number is K831635.

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

ACU-PUNCH received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831635.

Who is the listed applicant for ACU-PUNCH?

The FDA 510(k) record lists Acuderm, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Acuderm, Inc. as applicant

K933516ACU-E PUNCH K933265ACU-DISPO-CE(TM)K933137ACU-SUTURE KIT K930043ACU-EVAC K933866ACU-HEMOSTATIC RING K915000ACU-GUARD

View all 13 devices →

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.