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The Kendall Company, L.P.

FDA Regulatory Profile

The Kendall Company, L.P. 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 January 31, 2000.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K990530KERLIX MD ANTIMICROBIAL GAUZE DRESSINGJanuary 31, 2000
K992079KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325September 29, 1999

FDA data resources