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Rahn Laboratories
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K900266
STERILE CARBON STEEL SURGICAL BLADE
March 1, 1990
K892461
NON-STERILE LATEX EXAMINATION GLOVES
July 28, 1989
K881479
OPERATION ROOM TOWEL
April 14, 1988