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HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001

Page Type
Cleared 510(K)
510(k) Number
K021916
510(k) Type
Traditional
Applicant
HARMAC MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2002
Days to Decision
79 days
Submission Type
Summary

HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001

Page Type
Cleared 510(K)
510(k) Number
K021916
510(k) Type
Traditional
Applicant
HARMAC MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2002
Days to Decision
79 days
Submission Type
Summary