The following data is part of a premarket notification filed by Wahl Clipper Corp. with the FDA for Wahl Fresh Face.
| Device ID | K944909 |
| 510k Number | K944909 |
| Device Name: | WAHL FRESH FACE |
| Classification | Vibrator, Therapeutic |
| Applicant | WAHL CLIPPER CORP. 2900 NORTH LOCUST ST. P.O. BOX 578 Steriling, IL 61081 -0578 |
| Contact | Cynthia De Long |
| Correspondent | Cynthia De Long WAHL CLIPPER CORP. 2900 NORTH LOCUST ST. P.O. BOX 578 Steriling, IL 61081 -0578 |
| Product Code | IRO |
| CFR Regulation Number | 890.5975 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-10-05 |
| Decision Date | 1995-05-08 |