The following data is part of a premarket notification filed by Alko Diagnostic Corp. with the FDA for Reagents For Abbott Spectrum/epx (electro Calibra).
Device ID | K925385 |
510k Number | K925385 |
Device Name: | REAGENTS FOR ABBOTT SPECTRUM/EPX (ELECTRO CALIBRA) |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | ALKO DIAGNOSTIC CORP. ALKO PARK 333 FISKE ST. Holliston, MA 01746 |
Contact | Brian J Young |
Correspondent | Brian J Young ALKO DIAGNOSTIC CORP. ALKO PARK 333 FISKE ST. Holliston, MA 01746 |
Product Code | JIX |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-10-26 |
Decision Date | 1994-01-13 |