The following data is part of a premarket notification filed by Datex Division Instrumentarium Corp. with the FDA for Capnomac Ultima Anesthesia Monitor.
Device ID | K923276 |
510k Number | K923276 |
Device Name: | CAPNOMAC ULTIMA ANESTHESIA MONITOR |
Classification | Analyzer, Gas, Enflurane, Gaseous-phase (anesthetic Concentration) |
Applicant | DATEX DIVISION INSTRUMENTARIUM CORP. P.O. BOX 446 SF-00101 Helsinki, Finland, FI |
Contact | Antti Ritvos |
Correspondent | Antti Ritvos DATEX DIVISION INSTRUMENTARIUM CORP. P.O. BOX 446 SF-00101 Helsinki, Finland, FI |
Product Code | CBQ |
CFR Regulation Number | 868.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-06 |
Decision Date | 1993-07-21 |