VETA/VENTED ESOPHAGEAL TUBE AIRWAY— 510(k) K864200

Substantially Equivalent

Cranco Co.

FDA 510(k) clearance K864200 for VETA/VENTED ESOPHAGEAL TUBE AIRWAY, Substantially Equivalent on 1987-03-17. Applicant: Cranco Co.. Device class: 2.

Clearance details

Applicant: Cranco Co.
Product code: Code CAO
Device class: Class 2
Regulation: 21 CFR 868.5650
Advisory panel: Anesthesiology
Date received: 1986-10-27
Decision date: 1987-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Recent devices under product code CAO

K971348 — FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEM1998-02-27
K894032 — EVAC-TUBE1989-08-31
K875226 — ESOPHAGEAL OBTURATOR/TRACHEAL TUBE1988-01-19
K863172 — RESPIRONICS PTL REVIVEEASY1986-11-04
K761195 — ESOPHAGEAL OBTURATION AIRWAY1976-12-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.