The following data is part of a premarket notification filed by Medicor Usa Ltd. with the FDA for Cpm Metabolic Monitor.
Device ID | K823695 |
510k Number | K823695 |
Device Name: | CPM METABOLIC MONITOR |
Classification | Computer, Oxygen-uptake |
Applicant | MEDICOR USA LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | BZL |
CFR Regulation Number | 868.1730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-12-08 |
Decision Date | 1983-01-14 |