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RESPIRATION MONITOR 1000

Page Type
Cleared 510(K)
510(k) Number
K820778
510(k) Type
Traditional
Applicant
INTL. MEDICAL DEVICES LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1982
Days to Decision
41 days

RESPIRATION MONITOR 1000

Page Type
Cleared 510(K)
510(k) Number
K820778
510(k) Type
Traditional
Applicant
INTL. MEDICAL DEVICES LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1982
Days to Decision
41 days