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Boehringer Laboratories

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
43
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243399Boehringer Laboratories Liver RetractorJuly 2, 2025
K234033ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)May 6, 2024
K234145ViSiGi 3D Gastric Sizing TubeJanuary 26, 2024
K151990Tissue Removal SystemSeptember 11, 2015
K150781Tissue Removal PouchJune 19, 2015
K130483BOEHRINGER GASTRIC SIZING TUBEMarch 28, 2013
K061788BOEHRINGER LABORATORIES SUCTION PUMP SYSTEMJuly 11, 2006
K060277BOEHRINGER LABORATORIES SUCTION PUMP SYSTEMMarch 3, 2006
K020538BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIESMay 15, 2002
K014187AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEMFebruary 6, 2002
K013976BOEHRINGER MRI SUCTION REGULATORYJanuary 8, 2002
K955010AUTOVAC BP SYSTE, 2000 SERIESJune 20, 1996
K945775BOEHRINGER AUTOVAC(R) 7900 SERIESOctober 19, 1995
K932093AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 SJuly 6, 1994
K933232BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIEDMarch 28, 1994
K930615AUTOVAC CLOSED WOUND SUCTION SYSTEMFebruary 22, 1994
K934390OSCILLATING BONE SAW BLADE, 6200 SERIESJanuary 26, 1994
K924894AUTOVAC 7900 SERIESFebruary 5, 1993
K924953FLUID COOLED BONE SAW BLADE, 6000 SERIESJanuary 21, 1993
K904164AUTOVAC (R) AUTOTRANSFUSION SYSTEM, 7900 MODIFIEDSeptember 6, 1991