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The Traumafuse Co.

FDA Regulatory Profile

The Traumafuse Co. 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 January 9, 1990.

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

FDA data resources