Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by LIFETEK MEDICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K992308
07/09/1999
OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138
LIFETEK MEDICAL, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact