510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K090167Substantially Equivalent

Philips Avent Classic Stage 2 and 3 Teether, Model Scf882/01, Scf884/01, Philips Avent Animal Stage 2 and 3 Teether,

Philips Electronics UK Limited, Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K090167 is the FDA 510(k) clearance record for PHILIPS AVENT CLASSIC STAGE 2 AND 3 TEETHER, MODEL SCF882/01, SCF884/01, PHILIPS AVENT ANIMAL STAGE 2 AND 3 TEETHER,, a class II device, cleared for Philips Electronics UK Limited on under FDA product code KKO (Ring, Teething, Fluid-Filled). FDA records list 3 510(k) clearances for Philips Electronics UK Limited, from to . As of , FDA records show no recalls naming K090167.

Clearance record

Decision date
Received
(147 days to decision)
Product code
KKO Ring, Teething, Fluid-Filled
Regulation
21 CFR 872.5550
Device class
Class II
Review panel
Dental
Applicant
Philips Electronics UK Limited 10306 Chevy Chase Dr., Houston TX
510(k) summary
Statement
Third party review
No

Clearances, product code KKO

Trailing 12 months

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

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