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WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031622
510(k) Type
Traditional
Applicant
PORTEX LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/26/2003
Days to Decision
34 days
Submission Type
Summary

WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031622
510(k) Type
Traditional
Applicant
PORTEX LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/26/2003
Days to Decision
34 days
Submission Type
Summary