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FDA 510(k)

ONE TIME COMPOUND BENZOIN TINCTURE-

K-Number: K833120 · 1983-12-29

ApplicantAcme United Corp.
Decision Date1983-12-29
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ONE TIME COMPOUND BENZOIN TINCTURE- 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 1983-12-29 under 510(k) number K833120. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE TIME COMPOUND BENZOIN TINCTURE-?

ONE TIME COMPOUND BENZOIN TINCTURE- is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Acme United Corp.. The 510(k) number is K833120.

When did ONE TIME COMPOUND BENZOIN TINCTURE- receive FDA 510(k) clearance?

ONE TIME COMPOUND BENZOIN TINCTURE- received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833120.

Who is the listed applicant for ONE TIME COMPOUND BENZOIN TINCTURE-?

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 ONE TIME COMPOUND BENZOIN TINCTURE-?

The FDA product code for ONE TIME COMPOUND BENZOIN TINCTURE- is KGX.

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Related Devices (Code: KGX)

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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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