The following data is part of a premarket notification filed by Mortara Instrument, Inc. with the FDA for Model El-1 W/st Monitor Option (acronym = Eli/stm).
Device ID | K864580 |
510k Number | K864580 |
Device Name: | MODEL EL-1 W/ST MONITOR OPTION (ACRONYM = ELI/STM) |
Classification | Electrocardiograph |
Applicant | MORTARA INSTRUMENT, INC. 7865 NORTH 86TH ST. Milwaukee, WI 53224 |
Contact | Timothy C Mickelson |
Correspondent | Timothy C Mickelson MORTARA INSTRUMENT, INC. 7865 NORTH 86TH ST. Milwaukee, WI 53224 |
Product Code | DPS |
CFR Regulation Number | 870.2340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-11-20 |
Decision Date | 1987-02-20 |