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PROLOG MP PULSE GENERATORS 658K AND 658T

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872779
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1987
Days to Decision
113 days

PROLOG MP PULSE GENERATORS 658K AND 658T

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872779
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1987
Days to Decision
113 days