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Tri/Bor Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K904718
AERO-GEN NUBULIZER SYSTEM
April 1, 1991
K904717
MICRO-VENT NEBULIZER SYSTEM
April 1, 1991
K904715
OXYGEN/AIR TUBING
January 2, 1991
K904716
AERO-GEN NEBULIZER
January 2, 1991
K904719
DISPOSABLE FACE MASK
January 2, 1991