The following data is part of a premarket notification filed by Hgm Medical Laser Systems, Inc. with the FDA for Hgm Combination Nd:yag & Solid State Green.
Device ID | K910272 |
510k Number | K910272 |
Device Name: | HGM COMBINATION ND:YAG & SOLID STATE GREEN |
Classification | Powered Laser Surgical Instrument |
Applicant | HGM MEDICAL LASER SYSTEMS, INC. 3959 WEST 1820 SOUTH Salt Lake City, UT 84104 |
Contact | Dennis Reigle |
Correspondent | Dennis Reigle HGM MEDICAL LASER SYSTEMS, INC. 3959 WEST 1820 SOUTH Salt Lake City, UT 84104 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-01-23 |
Decision Date | 1991-08-09 |