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GUARDED NEEDLE 2000

Page Type
Cleared 510(K)
510(k) Number
K003406
510(k) Type
Traditional
Applicant
INTERNATIONAL MEDICAL DEVICE PARTNERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2001
Days to Decision
72 days
Submission Type
Statement

GUARDED NEEDLE 2000

Page Type
Cleared 510(K)
510(k) Number
K003406
510(k) Type
Traditional
Applicant
INTERNATIONAL MEDICAL DEVICE PARTNERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2001
Days to Decision
72 days
Submission Type
Statement