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DRM 2300 PLETHYSMOGRAPHIC CARDIOTACHOMETER

Page Type
Cleared 510(K)
510(k) Number
K871149
510(k) Type
Traditional
Applicant
IONTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1987
Days to Decision
74 days

DRM 2300 PLETHYSMOGRAPHIC CARDIOTACHOMETER

Page Type
Cleared 510(K)
510(k) Number
K871149
510(k) Type
Traditional
Applicant
IONTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1987
Days to Decision
74 days