510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K864200Substantially Equivalent

Veta/vented Esophageal Tube Airway

Cranco Co., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864200 is the FDA 510(k) clearance record for VETA/VENTED ESOPHAGEAL TUBE AIRWAY, a class II device, cleared for Cranco Co. on under FDA product code CAO (Airway, Esophageal (Obturator)). FDA records list one 510(k) clearance for Cranco Co. As of , FDA records show no recalls naming K864200.

Clearance record

Decision date
Received
(141 days to decision)
Product code
CAO Airway, Esophageal (Obturator)
Regulation
21 CFR 868.5650
Device class
Class II
Review panel
Anesthesiology
Applicant
Cranco Co. 120 Oakwood Plz., Salt Lake City UT
Third party review
No

Clearances, product code CAO

Trailing 12 months

FDA records hold no clearances under product code CAO in the trailing twelve months.

FDA records show no clearances under product code CAO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260