Cleared Traditional

K123724 - DERMISEB CREAM

K123724 · Igi Laboratories, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Aug 2013
Decision
267d
Days
-
Risk

K123724 is an FDA 510(k) clearance for the DERMISEB CREAM. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Igi Laboratories, Inc. (Buena, US). The FDA issued a Cleared decision on August 28, 2013 after a review of 267 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K123724

510(k) Number K123724 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 04, 2012
Decision Date August 28, 2013
Days to Decision 267 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
152d slower than avg
Panel avg: 115d · This submission: 267d
Pathway characteristics
Predicate-based equivalence.

FRO Device Classification - Class 0,

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Consultant

Beach Products, Inc.
Marc D. Wita

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - FRO Dressing, Wound, Drug

All 649
Devices cleared under the same product code (FRO) and FDA review panel - the closest regulatory comparables to K123724.
HYALMIX CREAM
K123678 · Igi Laboratories, Inc. · Dec 2013
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K123910 · Neilmed Pharmaceuticals, Inc. · Oct 2013
PRONTOSAN WOUND GEL X
K130857 · B.Braun Medical, Inc. · Oct 2013
PROTHELIAL
K123904 · Mueller Medical International, LLC · Aug 2013
NEUTROPHASE(R) SKIN AND WOUND CLEANSER OTC
K131542 · Novabay Pharmaceuticals, Inc. · Jul 2013
ABSOCLEAR
K130553 · Pharmaplast S.A.E. · Jul 2013
K123724 · DERMISEB CREAM
Download PDF FDA Summary Igi Laboratories, Inc.