Last synced on 14 November 2025 at 11:06 pm

MODIFIED SOFTOUCH INTRODUCER W/HEMO VALVE & SIDE

Page Type
Cleared 510(K)
510(k) Number
K894445
510(k) Type
Traditional
Applicant
MALLINCKROOT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1989
Days to Decision
77 days

MODIFIED SOFTOUCH INTRODUCER W/HEMO VALVE & SIDE

Page Type
Cleared 510(K)
510(k) Number
K894445
510(k) Type
Traditional
Applicant
MALLINCKROOT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1989
Days to Decision
77 days