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PK-141 PATIENT CABLE

Page Type
Cleared 510(K)
510(k) Number
K083674
510(k) Type
Traditional
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2009
Days to Decision
111 days
Submission Type
Summary

PK-141 PATIENT CABLE

Page Type
Cleared 510(K)
510(k) Number
K083674
510(k) Type
Traditional
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2009
Days to Decision
111 days
Submission Type
Summary