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Inntec, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K052059IUI CATHETER, MODEL 9057November 22, 2005
K051742OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SHOctober 7, 2005
K050521EMBRYO TRANSFER CATHETER WITH ACCESSORY STYLET, MODELS 9018, 9023, 9018-S, 9023-SMay 2, 2005