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ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102274
510(k) Type
Traditional
Applicant
Arvik Enterprises/ Mini Lap Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2011
Days to Decision
308 days
Submission Type
Summary

ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102274
510(k) Type
Traditional
Applicant
Arvik Enterprises/ Mini Lap Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2011
Days to Decision
308 days
Submission Type
Summary