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FDA 510(k)

SURGI-SCRUB V

K-Number: K822865 · 1982-10-18

ApplicantAcme United Corp.
Decision Date1982-10-18
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGI-SCRUB V is the device name listed in this FDA 510(k) record. The listed applicant is Acme United Corp.. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K822865. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGI-SCRUB V?

SURGI-SCRUB V is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Acme United Corp.. The 510(k) number is K822865.

When did SURGI-SCRUB V receive FDA 510(k) clearance?

SURGI-SCRUB V received FDA 510(k) clearance on 1982-10-18, under 510(k) number K822865.

Who is the listed applicant for SURGI-SCRUB V?

The FDA 510(k) record lists Acme United Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGI-SCRUB V?

The FDA product code for SURGI-SCRUB V is GEC.

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Other records listing Acme United Corp. as applicant

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Related Devices (Code: GEC)

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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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