Cleared Traditional

K111168 - PRECISION SKIN EMULSION

K111168 · Precision Dermatology Incorporated · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2011
Decision
232d
Days
-
Risk

K111168 is an FDA 510(k) clearance for the PRECISION SKIN EMULSION. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Precision Dermatology Incorporated (Cumberland, US). The FDA issued a Cleared decision on December 13, 2011 after a review of 232 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.

View all Precision Dermatology Incorporated devices

FDA 510(k) Submission Details - K111168

510(k) Number K111168 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 2011
Decision Date December 13, 2011
Days to Decision 232 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
117d slower than avg
Panel avg: 115d · This submission: 232d
Pathway characteristics
Predicate-based equivalence.

FRO Device Classification - Class 0,

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

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