Viasys Medsystems

FDA Regulatory Profile

Viasys Medsystems appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 7, 2008.

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K081725ENTERAL PUMP SET, MODEL 20-1010November 7, 2008
K080679MODIFICATION TO CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900June 27, 2008
K063061CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900April 2, 2007
K043044ANTI-I.V. ENTERAL FEEDING SYSTEMMay 6, 2005
K050309PULMANEX DISPOSABLE PRESSURE MANOMETER, MODEL 50-5000March 25, 2005
K043004STACKHOUSE FREEDOMAIRE II SURGICAL HELMET SYSTEM, MODELS 12000, 12010, 12011, 12020, 12021, 12022, 1March 16, 2005
K041987CORTRAKDecember 17, 2004