Atlas FDA

Capintec Inc

6 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Capintec Inc

RecordFirmDate
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usag recall (Z-1564-2020)Capintec Inc2020-03-24
Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077 recall (Z-0550-2019)Capintec Inc2018-12-04
Captus 700 Thyroid Uptake System, Model # 5430-3137 and 5430-3138 recall (Z-0551-2019)Capintec Inc2018-12-04
Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended to be used by tra recall (Z-2312-2012)Capintec Inc2012-09-05
Capintec CRC 25 PET, item number 5130-3217 with Software Revisions 2.01 and 2.02 PET dose recall (Z-0177-2012)Capintec Inc2011-11-09
Captus 3000 Thyroid Uptake System with Portable Stand option. Capintec item number 5430-21 recall (Z-0167-2011)Capintec Inc2010-10-28

Track Capintec Inc automatically

Every clearance here is in the API, with alerts when new ones post.