The following data is part of a premarket notification filed by Hgm Medical Laser Systems, Inc. with the FDA for Air Argon Ion Lasers Various Models.
Device ID | K912628 |
510k Number | K912628 |
Device Name: | AIR ARGON ION LASERS VARIOUS MODELS |
Classification | Powered Laser Surgical Instrument |
Applicant | HGM MEDICAL LASER SYSTEMS, INC. 3959 WEST 1820 SOUTH Salt Lake City, UT 84104 |
Contact | Gregory Mcarthur |
Correspondent | Gregory Mcarthur 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 | 1991-06-17 |
Decision Date | 1991-09-13 |