The following data is part of a premarket notification filed by Aequitron Medical, Inc. with the FDA for Model Number 8200 Respiration/heart Rate Monitor.
Device ID | K871551 |
510k Number | K871551 |
Device Name: | MODEL NUMBER 8200 RESPIRATION/HEART RATE MONITOR |
Classification | Monitor, Breathing Frequency |
Applicant | AEQUITRON MEDICAL, INC. 14800 28TH AVE. NORTH Minneapolis, MN 55447 -4834 |
Contact | Kenneth B Herland |
Correspondent | Kenneth B Herland AEQUITRON MEDICAL, INC. 14800 28TH AVE. NORTH Minneapolis, MN 55447 -4834 |
Product Code | BZQ |
CFR Regulation Number | 868.2375 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-22 |
Decision Date | 1987-06-05 |