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Akers Laboratories, Inc.

FDA Regulatory Profile

Akers Laboratories, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 28, 2004.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040293HEALTHTEST HEPARIN/PLATELET FACTOR 4 ANTIBODY ASSAYMay 28, 2004
K031579INSTAREAD LITHIUM SYSTEMDecember 19, 2003
K030815AKERS LABORATORIES INC. BLOOD CELL SEPARATORSeptember 17, 2003

FDA data resources