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SIDEPORT PINCH CLAMP DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010888
510(k) Type
Traditional
Applicant
MEDIVICE SYSTEMS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/27/2001
Days to Decision
96 days
Submission Type
Statement

SIDEPORT PINCH CLAMP DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010888
510(k) Type
Traditional
Applicant
MEDIVICE SYSTEMS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/27/2001
Days to Decision
96 days
Submission Type
Statement