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- PMIFluorescence In Situ Hybridization, Platelet-Derived Growth Factor Receptor, Beta Polypeptide (Pdgfrb), Rearrangement3Product Code
- PNKFluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)3Product Code
- QUESpinal Muscular Atrophy Newborn Screening Test System2Product Code
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EasySep™ Human Bone Marrow CD138 Positive Selection Kit (100-0748)
- Page Type
- Cleared 510(K)
- PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- DEN220090
- 510(k) Type
- Direct
- Applicant
- Stemcell Technologies Canada, Inc.
- Country
- Canada
- FDA Decision
- Deleted
- Decision Date
- 11/6/2023
- Days to Decision
- 329 days