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Hurricane Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K993361
TUBING EXTENSION SET
January 4, 2000
K990672
LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET
May 18, 1999
K990671
DRAINAGE WICK; SURGICAL SPEARS AND SPONGES, CORNEAL LIGHT SHIELD, INSTRUMENT WIPE
May 10, 1999