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Ross Product Div. Abbott Laboratories

FDA Regulatory Profile

Ross Product Div. Abbott Laboratories appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 20, 2003.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K031407ROSS EMBRACE ENTERAL PUMPMay 20, 2003
K003047AMBULATORY ENTERAL NUTRITION PUMPJune 12, 2001
K992494FLEXIFLO ENTERAL FEEDING TUBEAugust 25, 1999
K990863MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBEApril 6, 1999

FDA data resources