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Luxtec Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K973193LUXSCOPENovember 21, 1997
K970642TENOSCOPEMay 21, 1997
K970562TENOSNAREMay 14, 1997
K950960REDDY ILLUMINATORSeptember 8, 1995
K895248IMS5000 ILLUMINATED LOUPESSeptember 15, 1989
K890716LUXTEC ACO SERIES 4000 LIGHT SOURCEApril 26, 1989
K864387LUXTEC FIBEROPTIC CABLESMay 22, 1987
K864382FRAZIER SUCTION TUBEJanuary 14, 1987
K864383LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMSJanuary 14, 1987
K864385LUXTEC LIGHT SOURCESJanuary 13, 1987
K864865SPECULUM, VAGINAL, METAL FIBEROPTICJanuary 9, 1987
K864381LUXTEC VIDEOLUX 20/20 CAMERA HEADLIGHT SYSTEMDecember 9, 1986
K864384LUXTEC RETRACTORS, LUXTEC SPECIALTY RETRACTORSNovember 19, 1986
K864380LUTEX HEADLIGHT SYSTEMSNovember 19, 1986
K864386LUXTEC LOUPES FOR SURGICAL VISIONNovember 17, 1986