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FDA 510(k)

COMPOUND BENZOIN TINCTURE USP FREPP

K-Number: K920399 · 1994-01-25

ApplicantMedi-Flex Hospital Products, Inc.
Decision Date1994-01-25
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMPOUND BENZOIN TINCTURE USP FREPP is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Flex Hospital Products, Inc.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K920399. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPOUND BENZOIN TINCTURE USP FREPP?

COMPOUND BENZOIN TINCTURE USP FREPP is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Medi-Flex Hospital Products, Inc.. The 510(k) number is K920399.

When did COMPOUND BENZOIN TINCTURE USP FREPP receive FDA 510(k) clearance?

COMPOUND BENZOIN TINCTURE USP FREPP received FDA 510(k) clearance on 1994-01-25, under 510(k) number K920399.

Who is the listed applicant for COMPOUND BENZOIN TINCTURE USP FREPP?

The FDA 510(k) record lists Medi-Flex Hospital Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPOUND BENZOIN TINCTURE USP FREPP?

The FDA product code for COMPOUND BENZOIN TINCTURE USP FREPP is KMF.

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Other records listing Medi-Flex Hospital Products, Inc. as applicant

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Related Devices (Code: KMF)

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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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