The following data is part of a premarket notification filed by Respitrace Corp. with the FDA for Respitrace System.
Device ID | K823782 |
510k Number | K823782 |
Device Name: | RESPITRACE SYSTEM |
Classification | Spirometer, Monitoring (w/wo Alarm) |
Applicant | RESPITRACE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | BZK |
CFR Regulation Number | 868.1850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-12-15 |
Decision Date | 1983-03-07 |