Halifax Biomedical, Inc.

FDA Regulatory Profile

Halifax Biomedical, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Oct 31, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K182880Halifax Imaging KitOct 31, 2018
K133966MODEL-BASED RSA SOFTWAREMar 6, 2014
K121345SR SUITE 1.0Jun 1, 2012
K103417HALIFAX BIOMEDICAL TANATLUM BEAD SETJun 28, 2011
K090581TANTALUM BEAD SET, MODEL P003175Aug 21, 2009