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Hana Biologics, Inc.

FDA Regulatory Profile

Hana Biologics, Inc. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Sep 16, 1988

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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) clearances8Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K883682CHANG MEDIUM (ADDITIONAL INDICATIONS)Sep 16, 1988
K855205MYCOTRIM TM VL TRIPHASIC CULTURE SYSTEMFeb 5, 1986
K834616AMNIO STAT-FLM AGGLUTINATION TESTMay 25, 1984
K833933ACE COLOR TESTMar 23, 1984
K822737MYCOTRIUM-RSDec 3, 1982
K822736MYCOTRIUM-GUDec 3, 1982
K822150AMNISTAT-FLMOct 21, 1982
K812820CHANG MEDIUMNov 10, 1981

FDA data resources