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GLOBAL BLASTOCYST VITRIFICATION KIT & VITRIFICATION THAWING KIT - BASED ON S3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092963
510(k) Type
Traditional
Applicant
GENX INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2011
Days to Decision
476 days
Submission Type
Statement

GLOBAL BLASTOCYST VITRIFICATION KIT & VITRIFICATION THAWING KIT - BASED ON S3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092963
510(k) Type
Traditional
Applicant
GENX INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2011
Days to Decision
476 days
Submission Type
Statement