Gyneco, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gyneco, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Gyneco, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1984 to 1986. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Gyneco, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gyneco, Inc.
5 devices
Cleared
May 05, 1986
SYNCARE TEMPORARY CARDIAC PACING WIRE
Cardiovascular
20d
Cleared
Apr 02, 1986
MASTER ENDOMET BIOPSY KIT W/PLAS CURE 3,4MM-4003,4
Obstetrics & Gynecology
244d
Cleared
Jul 05, 1985
GYNE-SHEAR CERVICAL BIOPSY INSTRUMENT W/DISPIS TIP
Obstetrics & Gynecology
32d
Cleared
Feb 25, 1985
ENDOCYTE
Obstetrics & Gynecology
139d
Cleared
Aug 17, 1984
FINE NEEDLE ASPIRATION DEVICE
Cardiovascular
143d