Last synced on 14 November 2025 at 11:06 pm

INTERJECTOR BLOOD COLLECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K901756
510(k) Type
Traditional
Applicant
BOWMAN/VECTOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1990
Days to Decision
134 days

INTERJECTOR BLOOD COLLECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K901756
510(k) Type
Traditional
Applicant
BOWMAN/VECTOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1990
Days to Decision
134 days