ESOPHAGEAL OBTURATOR/TRACHEAL TUBE— 510(k) K875226

Name: FDA 510(k) clearance K875226
Creator: U.S. Food and Drug Administration
Published: 1988-01-19

Substantially Equivalent

Sheridan Catheter Corp.

FDA 510(k) clearance K875226 for ESOPHAGEAL OBTURATOR/TRACHEAL TUBE, Substantially Equivalent on 1988-01-19. Applicant: Sheridan Catheter Corp.. Device class: 2.

Clearance details

Applicant: Sheridan Catheter Corp.
Product code: Code CAO
Device class: Class 2
Regulation: 21 CFR 868.5650
Advisory panel: Anesthesiology
Date received: 1987-12-22
Decision date: 1988-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Argyle, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAO

view all

K971348 — FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEM1998-02-27
K894032 — EVAC-TUBE1989-08-31
K864200 — VETA/VENTED ESOPHAGEAL TUBE AIRWAY1987-03-17
K863172 — RESPIRONICS PTL REVIVEEASY1986-11-04
K761195 — ESOPHAGEAL OBTURATION AIRWAY1976-12-09

More clearances from Sheridan Catheter Corp.

view all

K922894 — LAZER-TRACH TRACHEAL TUBE1993-05-07
K897046 — LASER RESISTANT TRACHEAL TUBE1990-03-23
K890823 — ACCESSORY TO CLINICAL ELECTRONIC THERMOMETER1989-05-05
K884765 — CLINICAL ELECTRONIC THERMOMETERS1989-02-16
K882918 — KIM NASO-INTESTINAL TUBE1988-12-05

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