Last synced on 25 January 2026 at 3:41 am

HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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