Laser Spectrum, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laser Spectrum, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Laser Spectrum, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1984 to 1986. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Laser Spectrum, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laser Spectrum, Inc.
5 devices
Cleared
Oct 06, 1986
CO2 LASER MICROMANIPULATOR
Obstetrics & Gynecology
26d
Cleared
Apr 08, 1985
ACCESSORY SET FOR CO2 LASER BRONCHOSCOPY INSTRUMEN
Ear, Nose, Throat
122d
Cleared
Nov 07, 1984
MODEL 305AA PORTABLE LASER
General & Plastic Surgery
191d
Cleared
Sep 25, 1984
DANIELL DBL PUNCTURE LASER LAPAROSCOPY
Obstetrics & Gynecology
91d
Cleared
Apr 23, 1984
CO2 LAPAROSCOPE
Gastroenterology & Urology