The following data is part of a premarket notification filed by Phoenix Diagnostics, Inc. with the FDA for Phoenix Electrolyte Calibration Set For The Medical Easylyte Calcium Analyzer.
Device ID | K012987 |
510k Number | K012987 |
Device Name: | PHOENIX ELECTROLYTE CALIBRATION SET FOR THE MEDICAL EASYLYTE CALCIUM ANALYZER |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | PHOENIX DIAGNOSTICS, INC. 8 TECH CIRCLE Natick, MA 01760 |
Contact | Ram Nunna |
Correspondent | Ram Nunna PHOENIX DIAGNOSTICS, INC. 8 TECH CIRCLE Natick, MA 01760 |
Product Code | JIX |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-09-06 |
Decision Date | 2001-11-07 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00853366007615 | K012987 | 000 |
00853366007608 | K012987 | 000 |
00853366007585 | K012987 | 000 |