BICORE SMARTCATH INTRATRACHEAL CATHETER— 510(k) K935788

Substantially Equivalent

Bicore Monitoring Systems

FDA 510(k) clearance K935788 for BICORE SMARTCATH INTRATRACHEAL CATHETER, Substantially Equivalent on 1995-07-03. Applicant: Bicore Monitoring Systems. Device class: 2.

Clearance details

Applicant
Bicore Monitoring Systems
Product code
Code MOD
Device class
Class 2
Regulation
21 CFR 868.5895
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Irvine, CA, US
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