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CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961690
510(k) Type
Traditional
Applicant
CONTINENTAL X-RAY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
57 days
Submission Type
Statement

CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961690
510(k) Type
Traditional
Applicant
CONTINENTAL X-RAY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
57 days
Submission Type
Statement