Aspen Labs is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aspen Labs - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Aspen Labs has 6 FDA 510(k) cleared medical devices. Based in Utica, US.
Historical record: 6 cleared submissions from 1991 to 1997. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Aspen Labs Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aspen Labs
6 devices
Cleared
Apr 30, 1997
HYFRECATOR 2000
General & Plastic Surgery
79d
Cleared
Sep 27, 1994
SINGLE USE TUNGSTEN WIRE LEE LOOP ELECTRODE
Obstetrics & Gynecology
706d
Cleared
Mar 28, 1994
HAND-TROL S
General & Plastic Surgery
383d
Cleared
Mar 05, 1992
SINGLE USE LEE ELECTRODE
Obstetrics & Gynecology
302d
Cleared
Mar 18, 1991
ELECTROSURGICAL UNIT WITH ACCESSORIES
General & Plastic Surgery
90d
Cleared
Feb 19, 1991
SINGLE USE LAPARSCOPIC ELECTRODE
Obstetrics & Gynecology
159d