Baylis Medical Corp *
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| NRG Transseptal Needle and NRG RF Transseptal Kit. Model/Catalogue Numbers: NRG-56-32-C0, recall (Z-0393-2017) | Baylis Medical Corp * | 2016-11-10 |
| ProTrack Microcatheter. Model/Catalog Numbers CIC38-145, CIC35-145. Sterile, single use de recall (Z-0356-2016) | Baylis Medical Corp * | 2015-12-01 |
| ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use recall (Z-1442-2015) | Baylis Medical Corp * | 2015-04-13 |
| Baylis Medical TorFlex Transseptal Guiding Sheath, Rx Only, non-pyrogenic, sterile. Produc recall (Z-0085-2014) | Baylis Medical Corp * | 2013-11-01 |
| The Baylis LumbarCool Pain Management Kit consisting of: 1 LumbarCool Pain Management Prob recall (Z-1755-2010) | Baylis Medical Corp * | 2010-06-03 |
| Torflex Transseptal Guiding Sheath, Baylis Medical Company Inc., 5959 Trans-Canada Highway recall (Z-0816-2010) | Baylis Medical Corp * | 2010-03-10 |
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Every clearance here is in the API, with alerts when new ones post.