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Lifepoint,Inc
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K041747
IMPACT TEST SYSTEM SALIVA TEST MODULE-OPIATE (WORKPLACE)
November 24, 2004
K041746
IMPACT TEST SYSTEM; SALIVA TEST MODULE-OPIATE (PRESCRIPTION USE)
November 23, 2004
K833737
CPR LOCATOR
August 24, 1984