The following data is part of a premarket notification filed by Msq (m2) Ltd. with the FDA for Modified Msq Family Of Lovely Light/laser Systems.
| Device ID | K042000 |
| 510k Number | K042000 |
| Device Name: | MODIFIED MSQ FAMILY OF LOVELY LIGHT/LASER SYSTEMS |
| Classification | Powered Laser Surgical Instrument |
| 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 | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-07-26 |
| Decision Date | 2004-12-21 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 17290110121126 | K042000 | 000 |
| 17290110121072 | K042000 | 000 |