Last synced on 14 November 2025 at 11:06 pm

KONTRON PULSE OXIMETER 7840

Page Type
Cleared 510(K)
510(k) Number
K890299
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1989
Days to Decision
42 days

KONTRON PULSE OXIMETER 7840

Page Type
Cleared 510(K)
510(k) Number
K890299
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1989
Days to Decision
42 days