The following data is part of a premarket notification filed by Medical Laboratory Automation Systems, Inc. with the FDA for Mla Electra 750 Coagulation Timer.
Device ID | K780810 |
510k Number | K780810 |
Device Name: | MLA ELECTRA 750 COAGULATION TIMER |
Classification | System, Multipurpose For In Vitro Coagulation Studies |
Applicant | MEDICAL LABORATORY AUTOMATION SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JPA |
CFR Regulation Number | 864.5425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-05-18 |
Decision Date | 1978-06-14 |