The following data is part of a premarket notification filed by Medical Laboratory Automation Systems, Inc. with the FDA for Electra 1800c Automatic Coagulation Analyzer.
Device ID | K962664 |
510k Number | K962664 |
Device Name: | ELECTRA 1800C AUTOMATIC COAGULATION ANALYZER |
Classification | Instrument, Coagulation, Automated |
Applicant | MEDICAL LABORATORY AUTOMATION SYSTEMS, INC. 270 MARBLE AVE. Pleasantville, NY 10570 |
Contact | Joann H Lopez |
Correspondent | Joann H Lopez MEDICAL LABORATORY AUTOMATION SYSTEMS, INC. 270 MARBLE AVE. Pleasantville, NY 10570 |
Product Code | GKP |
CFR Regulation Number | 864.5400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-09 |
Decision Date | 1996-09-10 |
Summary: | summary |