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MIDSLEEVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142548
510(k) Type
Traditional
Applicant
MEDICAL INNOVATION DEVELOPMENT
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/23/2015
Days to Decision
286 days
Submission Type
Summary