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MAXIMA FILTERED HARDSHELL RESERVOIR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932254
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
8/3/1993
Days to Decision
85 days
Submission Type
Summary

MAXIMA FILTERED HARDSHELL RESERVOIR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932254
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
8/3/1993
Days to Decision
85 days
Submission Type
Summary