510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K892435Substantially Equivalent

Kendall Curity Oxygen Nasal Cannula

The Kendal Co., Boston MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K892435 is the FDA 510(k) clearance record for KENDALL CURITY OXYGEN NASAL CANNULA, a class I device, cleared for The Kendal Co. on under FDA product code CAT (Cannula, Nasal, Oxygen). FDA records list 63 510(k) clearances for The Kendal Co., from to . As of , FDA records show no recalls naming K892435.

Clearance record

Decision date
Received
(63 days to decision)
Product code
CAT Cannula, Nasal, Oxygen
Regulation
21 CFR 868.5340
Device class
Class I
Review panel
Anesthesiology
Applicant
The Kendal Co. One Federal St., Boston MA
Third party review
No

Clearances, product code CAT

Trailing 12 months

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

FDA records show no clearances under product code CAT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAT, 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