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Solo Pak Laboratories
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K851944
MAX-I-PROBE HANDPIECE
July 1, 1985
K841306
HEPARIN LOCK FLUSH SOLUTION USP KIT,100
June 4, 1984
K841305
HEPARIN LOCK FLUSH SOLUTION USP KIT
June 4, 1984
K841166
HEPARIN LOCK FLUSH PROCEDURE PACK
June 4, 1984