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Apex Metal, 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
K970363
HYDROTEC LOW AIR LOSS THERAPY BED
November 17, 1997
K970364
AIRTEC2 LOW AIR LOSS THERAPY BED
November 17, 1997
K970362
CARE TEC PORTABLE LOW AIR LOSS THERAPY SYSTEM
May 16, 1997