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