FDA 510(k) Applications Submitted by WALLAC, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| DEN990008 | 12/20/1999 | WALLAC NEONATAL BIOTINIDASE TEST KIT, MODELS NB-1000; NB-4000 | WALLAC, INC. |
| K982307 | 07/01/1998 | WALLAC NEONATAL LEUCINE TEST KIT MODEL NL-1000 | WALLAC, INC. |
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