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SLEEP PAT 200 DEVICE

Page Type
Cleared 510(K)
510(k) Number
K010156
510(k) Type
Traditional
Applicant
ITAMAR MEDICAL (C.M.) 1997 LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2002
Days to Decision
519 days
Submission Type
Statement

SLEEP PAT 200 DEVICE

Page Type
Cleared 510(K)
510(k) Number
K010156
510(k) Type
Traditional
Applicant
ITAMAR MEDICAL (C.M.) 1997 LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2002
Days to Decision
519 days
Submission Type
Statement