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Thermedics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K894131
DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000
September 26, 1989
K863128
PERITONEAL DIALYSIS CATHETERS
September 9, 1986
K854966
ACUTE PERITONEAL DIALYSIS CATHETERS
January 9, 1986
K850076
WOUND DRESSING MODEL ZB-6
April 15, 1985