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INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940731
510(k) Type
Traditional
Applicant
INNERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1994
Days to Decision
207 days
Submission Type
Statement