Microquartz Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microquartz Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Microquartz Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Historical record: 6 cleared submissions from 1995 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Microquartz Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microquartz Medical, Inc.
6 devices
Cleared
Jan 26, 1996
MICROQUARTZ MEDICAL TYPE B SIDE-FIRING LASER FIBER
General & Plastic Surgery
30d
Cleared
Jan 22, 1996
MICROQUARTZ MEDICAL GENERAL SHAPE LASER FIBER
General & Plastic Surgery
89d
Cleared
Sep 27, 1995
ULTRABRIGHT (MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER)
General & Plastic Surgery
89d
Cleared
Aug 28, 1995
QUADRALASE (MICROQUARTZ MEDICAL ADJUSTABLE SIDE-FIRING LASER FIBER)
General & Plastic Surgery
62d
Cleared
Aug 28, 1995
MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY
General & Plastic Surgery
52d
Cleared
Mar 10, 1995
MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER
General & Plastic Surgery
25d