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PAJUNK DISPOSABLE BALLOONS AND BALLOON SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090631
510(k) Type
Traditional
Applicant
PAJUNK GMBH MEDIZINTECHNOLOGIE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/16/2009
Days to Decision
38 days
Submission Type
Summary