Cleared Traditional

MED CARE PREP RAZOR (K831374) - FDA 510(k) Clearance

K831374 · Medcare Products · General & Plastic Surgery device
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Oct 1983
Decision
160d
Days
-
Risk

K831374 is an FDA 510(k) clearance for the MED CARE PREP RAZOR.

Submitted by Medcare Products (Mchenry, US). The FDA issued a Cleared decision on October 4, 1983 after a review of 160 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.

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Submission Details

510(k) Number K831374 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 1983
Decision Date October 04, 1983
Days to Decision 160 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d slower than avg
Panel avg: 115d · This submission: 160d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -