Last synced on 14 November 2025 at 11:06 pm

KONTRON DEFIBRILLATOR 7501

Page Type
Cleared 510(K)
510(k) Number
K854307
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1985
Days to Decision
40 days

KONTRON DEFIBRILLATOR 7501

Page Type
Cleared 510(K)
510(k) Number
K854307
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1985
Days to Decision
40 days