The following data is part of a premarket notification filed by Datex Division Instrumentarium Corp. with the FDA for Datex As/3 Tm Anaesthesia Monitor.
Device ID | K933285 |
510k Number | K933285 |
Device Name: | DATEX AS/3 TM ANAESTHESIA MONITOR |
Classification | Gas-machine, Anesthesia |
Applicant | DATEX DIVISION INSTRUMENTARIUM CORP. 27 TEOLLISUUSKATU Helsinki, FI |
Contact | Hannu Ahjopalo |
Correspondent | Hannu Ahjopalo DATEX DIVISION INSTRUMENTARIUM CORP. 27 TEOLLISUUSKATU Helsinki, FI |
Product Code | BSZ |
CFR Regulation Number | 868.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-07-06 |
Decision Date | 1994-11-14 |