The following data is part of a premarket notification filed by Facemaster Of Beverly Hills, Inc. with the FDA for Facemaster Facial Toning System.
| Device ID | K040871 |
| 510k Number | K040871 |
| Device Name: | FACEMASTER FACIAL TONING SYSTEM |
| Classification | Stimulator, Transcutaneous Electrical, Aesthetic Purposes |
| Applicant | FACEMASTER OF BEVERLY HILLS, INC. THREE PARK PLAZA, SUITE 1570 Irvine, CA 92614 |
| Contact | Jim England |
| Correspondent | Jim England FACEMASTER OF BEVERLY HILLS, INC. THREE PARK PLAZA, SUITE 1570 Irvine, CA 92614 |
| Product Code | NFO |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-04-02 |
| Decision Date | 2005-06-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00879314000033 | K040871 | 000 |
| 00879314000026 | K040871 | 000 |