Last synced on 14 November 2025 at 11:06 pm

CONTRAST INJECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K880877
510(k) Type
Traditional
Applicant
MED-WEST, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1988
Days to Decision
91 days

CONTRAST INJECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K880877
510(k) Type
Traditional
Applicant
MED-WEST, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1988
Days to Decision
91 days