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LIFESCOPE 8, OEC-8120 PORTABLE PATIENT MONITOR REC

Page Type
Cleared 510(K)
510(k) Number
K862463
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1986
Days to Decision
158 days

LIFESCOPE 8, OEC-8120 PORTABLE PATIENT MONITOR REC

Page Type
Cleared 510(K)
510(k) Number
K862463
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1986
Days to Decision
158 days