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SYSTEM 7300 PULSE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K910521
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1991
Days to Decision
70 days

SYSTEM 7300 PULSE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K910521
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1991
Days to Decision
70 days