The following data is part of a premarket notification filed by Draeger Medical, Inc. with the FDA for Fabius Gs Anesthesia System; Fabius Tiro Anesthesia System.
Device ID | K042086 |
510k Number | K042086 |
Device Name: | FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEM |
Classification | Gas-machine, Anesthesia |
Applicant | DRAEGER MEDICAL, INC. 3135 QUARRY RD. Telford, PA 18969 |
Contact | Michael A Kelhart |
Correspondent | Michael A Kelhart DRAEGER MEDICAL, INC. 3135 QUARRY RD. Telford, PA 18969 |
Product Code | BSZ |
CFR Regulation Number | 868.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-03 |
Decision Date | 2004-08-31 |
Summary: | summary |