The following data is part of a premarket notification filed by Aequitron Medical, Inc. with the FDA for Medicon Model 8200 Ams(apnea Monitor System).
Device ID | K853084 |
510k Number | K853084 |
Device Name: | MEDICON MODEL 8200 AMS(APNEA MONITOR SYSTEM) |
Classification | Monitor, Breathing Frequency |
Applicant | AEQUITRON MEDICAL, INC. 14800 28TH AVE. NORTH Minneapolis, MN 55447 -4834 |
Contact | Robert C Samec |
Correspondent | Robert C Samec 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 | 1985-07-23 |
Decision Date | 1985-08-02 |