Alm Surgical Equipment, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K982063ALM PRISMALIX (PRX) SURGICAL LIGHTSeptember 22, 1998
K961886DRAGER GEMINA WALL-MOUNTED WORKPLACEJuly 30, 1996
K961742DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEMJuly 26, 1996
K945102MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCENovember 4, 1994
K942043DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032EJuly 13, 1994
K922409ALM ILLUMINATOR SERIES LIGHT SYSTEMJanuary 12, 1993
K921297DRAGER DVE 4000 SERIES SYSTEMNovember 27, 1992
K921848BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHTOctober 1, 1992
K884019ALM OPERATING TABLESOctober 13, 1988
K882613ALM SURGICAL LAMPSJuly 18, 1988