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Gabriel Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K960173INFRA VISION BOUGIE KIT, INFRA VISION ESOPHAGEAL KITJune 27, 1996
K945088GABRIEL URETERAL ILLUMINATOR SYSTEM IIFebruary 7, 1995
K945297INFRA VISION IMAGING SYSTEMDecember 20, 1994
K940019GABRIEL URETERAL ILLUMINATOR SYSTEMMay 2, 1994
K901385GABRIEL MEDICAL CLS THERMAL RECORDERMay 9, 1990