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FDA 510(k)

IODOFLEX PASTE

K-Number: K940414 · 1994-04-28

ApplicantOclassen Pharmaceuticals, Inc.
Decision Date1994-04-28
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

IODOFLEX PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Oclassen Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1994-04-28 under 510(k) number K940414. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the IODOFLEX PASTE?

IODOFLEX PASTE is a medical device that received FDA 510(k) clearance on 1994-04-28. The listed applicant is Oclassen Pharmaceuticals, Inc.. The 510(k) number is K940414.

When did IODOFLEX PASTE receive FDA 510(k) clearance?

IODOFLEX PASTE received FDA 510(k) clearance on 1994-04-28, under 510(k) number K940414.

Who is the listed applicant for IODOFLEX PASTE?

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

What is the FDA product code for IODOFLEX PASTE?

The FDA product code for IODOFLEX PASTE is KMF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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