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IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071883
510(k) Type
Special
Applicant
Cyden Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/23/2008
Days to Decision
198 days
Submission Type
Statement

IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071883
510(k) Type
Special
Applicant
Cyden Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/23/2008
Days to Decision
198 days
Submission Type
Statement