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The Traumafuse Co.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K895162TRAUMAFUSE TRACH SHIELDJanuary 9, 1990
K894721TRAUMAFUSE PERFUSION PRESSURE RELIEF VALVEOctober 20, 1989
K895132CONNELL-STEPHENS ENDO ANESS TUBEOctober 13, 1989
K890077TRAUMAFUSE RAPID INFUSION DEVICEApril 3, 1989