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Vesta, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
5
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K834078
SILICONE RUGGER DISPOSABLE YOKE-CPAP
December 27, 1983
K810960
NASOPHARYNGEAL AIRWAY
April 23, 1981
K792719
3 WAY URETHRAL IRRIGATION CATHETER
January 16, 1980
K792018
SILICONE RUBBER-BI NASOPHARYNGEAL AIR
November 13, 1979