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Labotect Labor-Technik Gottingen

FDA Regulatory Profile

Labotect Labor-Technik Gottingen appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 16, 2002.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K021438INSEMINATION CATHETER, MODEL 320301July 16, 2002
K003056OVARIAL BIOPSY SET 324102-324108; OVARIAL BIOPSY SET 324200-324202; OVARIAL BIOPSY NEEDLE 32218December 13, 2000
K000950EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201May 12, 2000

FDA data resources