Cleared Traditional

WAHL FRESH FACE

K944909 · Wahl Clipper Corp. · Physical Medicine
May 1995
Decision
215d
Days
Class 1
Risk

About This 510(k) Submission

K944909 is an FDA 510(k) clearance for the WAHL FRESH FACE, a Vibrator, Therapeutic (Class I — General Controls, product code IRO), submitted by Wahl Clipper Corp. (Steriling, US). The FDA issued a Cleared decision on May 8, 1995, 215 days after receiving the submission on October 5, 1994. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.5975.

Submission Details

510(k) Number K944909 FDA.gov
FDA Decision Cleared SESE
Date Received October 05, 1994
Decision Date May 08, 1995
Days to Decision 215 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

Device Classification

Product Code IRO — Vibrator, Therapeutic
Device Class Class I — General Controls
CFR Regulation 21 CFR 890.5975

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