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SPACELABS SERIES 600 PATIENT MONITORS

Page Type
Cleared 510(K)
510(k) Number
K844888
510(k) Type
Traditional
Applicant
SPACELABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1985
Days to Decision
46 days

SPACELABS SERIES 600 PATIENT MONITORS

Page Type
Cleared 510(K)
510(k) Number
K844888
510(k) Type
Traditional
Applicant
SPACELABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1985
Days to Decision
46 days