F.M. Wiest USA, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K921871HYSTEROMAT(TM) 3700December 15, 1994
K920574CAMSYS 6300February 17, 1993
K920575MERKUR 4000July 23, 1992
K915751URETEROMAT 4400April 24, 1992
K911844HYSTEROFLATOR 1500November 21, 1991
K912071SPACE(TM) 7500July 9, 1991
K910883LAPAROFLATOR ELECTRONIC 3509March 29, 1991
K875137LAPAROFLATOR 3000, STANDARD AND ELECTRONICMarch 2, 1988
K871181ARTHROCOMBI 5003September 29, 1987
K871180ARTHRO AUTOMAT 5002September 29, 1987
K865066ARTHROFLATORApril 20, 1987
K860571F.M. WEIST,KG (URODYNAMIC SYSTEMS)March 18, 1986