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Triton Technology, Inc.

FDA Regulatory Profile

Triton Technology, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 24, 1993.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K932142SUCTION GUILLOTINE DEVICESeptember 24, 1993
K911448MULTIPLE BIOPSY DEVICE-MBXApril 16, 1991
K902883TISSUE/POLYP TRAP SYSTEMSeptember 12, 1990
K881303TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETERNovember 29, 1988

FDA data resources