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Lifetek Medical, Inc.

FDA Regulatory Profile

Lifetek Medical, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 13, 1999.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992308OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138September 13, 1999
K921518LIFETEK IUI CATHETERMay 10, 1994

FDA data resources