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CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950210
510(k) Type
Traditional
Applicant
CARDIAC CONTROL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
5/3/1995
Days to Decision
104 days
Submission Type
Summary

CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950210
510(k) Type
Traditional
Applicant
CARDIAC CONTROL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
5/3/1995
Days to Decision
104 days
Submission Type
Summary