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QUICK SWITCH LAPAROSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932648
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1993
Days to Decision
132 days
Submission Type
Statement