The following data is part of a premarket notification filed by Liquid Air Corp. with the FDA for Anesthetic Gas Calibration Mixture.
Device ID | K902754 |
510k Number | K902754 |
Device Name: | ANESTHETIC GAS CALIBRATION MIXTURE |
Classification | Gas, Calibration (specified Concentration) |
Applicant | LIQUID AIR CORP. 1150 17TH STREET, N.W. SUITE 1000 Washington, DC 20036 |
Contact | Mark L Itzkoff |
Correspondent | Mark L Itzkoff LIQUID AIR CORP. 1150 17TH STREET, N.W. SUITE 1000 Washington, DC 20036 |
Product Code | BXK |
CFR Regulation Number | 868.6400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-06-22 |
Decision Date | 1990-12-19 |