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Medical Laser, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K913136LASER ENDOSCOPE DISC DECOMPRESSION KITSNovember 1, 1991
K912265MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000October 10, 1991
K912447SERIES 5000 ENDOSCOPE CONSOLE MODELS 5100 AND 5200September 27, 1991
K912089MODIFIED SERIES 2100 ENDOSCOPESAugust 12, 1991
K901464MEDILASE SERIES 2200 ENDOSCOPEAugust 7, 1990
K900894MEDILASE SERIES 2100 ENDOSCOPEJune 22, 1990
K900380MEDILASE 5010 ENDOSCOPE CONSOLEMay 15, 1990
K895837MEDILASE SYSTEM 2010L LASER LITHOTRIPTORDecember 14, 1989