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HR-2000 W/SUFFIXES B,C,D, CARDIO & DIGI LOOP, DDVP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882175
510(k) Type
Traditional
Applicant
EIGEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1988
Days to Decision
87 days

HR-2000 W/SUFFIXES B,C,D, CARDIO & DIGI LOOP, DDVP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882175
510(k) Type
Traditional
Applicant
EIGEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1988
Days to Decision
87 days