The following data is part of a premarket notification filed by Wallac Oy with the FDA for Delfia Neonatal Irt Kit.
Device ID | K993697 |
510k Number | K993697 |
Device Name: | DELFIA NEONATAL IRT KIT |
Classification | Electrode, Ion-specific, Chloride |
Applicant | WALLAC OY MUSTIONKATU 6 Turku, FI 20750 |
Contact | Gunnel Laaksonen |
Correspondent | Gunnel Laaksonen WALLAC OY MUSTIONKATU 6 Turku, FI 20750 |
Product Code | CGZ |
CFR Regulation Number | 862.1170 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-11-02 |
Decision Date | 2000-06-09 |
Summary: | summary |