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Nutec, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K940257
HAND-HELD NEBULIZER
October 13, 1994
K940255
HYPERINFLATION BAG SYSTEM
February 17, 1994
K935821
DOUBLE TRACH SWIVEL CONNECTOR
January 14, 1994