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OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992308
510(k) Type
Traditional
Applicant
LIFETEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1999
Days to Decision
66 days
Submission Type
Summary

OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992308
510(k) Type
Traditional
Applicant
LIFETEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1999
Days to Decision
66 days
Submission Type
Summary