510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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CAOClass II

Airway, Esophageal (Obturator)

21 CFR 868.5650 / Anesthesiology
FDA source (opens on fda.gov)

CAO is the FDA product code for Airway, Esophageal (Obturator), a class II device type, regulated under 21 CFR 868.5650. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CAO
Device name
Airway, Esophageal (Obturator)
Regulation
21 CFR 868.5650
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
6
Ingested recalls
0

Clearances, product code CAO

By decision year
6 clearances under product code CAO with a decision year between 1976 and 1998, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CAO by decision year
YearClearances
19761
19861
19871
19881
19891
19981

Applicants with the most clearances

Product code CAO
Applicants holding the most 510(k) clearances under product code CAO
ApplicantClearances
Cranco Co.1
Green Field Medical Sourcing, Inc.1
Mckesson Corp.1
Respironics, Inc.1
Sharn, Inc.1
Sheridan Catheter Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code