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HEARTHWATCH III(TM)

Page Type
Cleared 510(K)
510(k) Number
K945476
510(k) Type
Traditional
Applicant
INSTROMEDIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1995
Days to Decision
366 days
Submission Type
Statement

HEARTHWATCH III(TM)

Page Type
Cleared 510(K)
510(k) Number
K945476
510(k) Type
Traditional
Applicant
INSTROMEDIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1995
Days to Decision
366 days
Submission Type
Statement