Baro-Therapies, Inc

FDA Regulatory Profile

Baro-Therapies, Inc appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2734-2014, Class II) was initiated on August 8, 2014.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2734-2014Class IIThe Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relieAugust 8, 2014