The following data is part of a premarket notification filed by Msq (m2) Ltd. with the FDA for Lovely System.
| Device ID | K033946 |
| 510k Number | K033946 |
| Device Name: | LOVELY SYSTEM |
| Classification | Light, Ultraviolet, Dermatological |
| Applicant | MSQ (M2) LTD. 3637 BERNAL AVENUE Pleasanton, CA 94566 |
| Contact | Anne Worden |
| Correspondent | Anne Worden MSQ (M2) LTD. 3637 BERNAL AVENUE Pleasanton, CA 94566 |
| Product Code | FTC |
| CFR Regulation Number | 878.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-19 |
| Decision Date | 2004-04-05 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 17290110120457 | K033946 | 000 |
| 17290110120440 | K033946 | 000 |
| 17290110120433 | K033946 | 000 |