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NEEDLELESS TRANSFER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K001831
510(k) Type
Traditional
Applicant
MEDIMOP MEDICAL PROJECTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2000
Days to Decision
25 days
Submission Type
Statement

NEEDLELESS TRANSFER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K001831
510(k) Type
Traditional
Applicant
MEDIMOP MEDICAL PROJECTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2000
Days to Decision
25 days
Submission Type
Statement