Spiess Design, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spiess Design, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Spiess Design, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1979 to 1996. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Spiess Design, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spiess Design, Inc.
4 devices
Cleared
Jul 01, 1996
SAFETY TROCER WITH SPRINGLOADED OBDURATOR
Obstetrics & Gynecology
158d
Cleared
Apr 06, 1992
CO2 INSUFFLATOR HIGH FLOW ELECTRONIC INSUFFLATOR
Obstetrics & Gynecology
87d
Cleared
Nov 29, 1991
HYDRODISECTOR
General & Plastic Surgery
72d
Cleared
Jun 27, 1979
DELTA PUMP
General Hospital
61d