Last synced on 30 May 2025 at 11:05 pm

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