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
K830571Substantially Equivalent

Bottle Adapter

Burron Medical Products, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830571 is the FDA 510(k) clearance record for BOTTLE ADAPTER, a class I device, cleared for Burron Medical Products, Inc. on under FDA product code KYX (Dispenser, Liquid Medication). FDA records list 41 510(k) clearances for Burron Medical Products, Inc., from to . As of , FDA records show no recalls naming K830571.

Clearance record

Decision date
Received
(29 days to decision)
Product code
KYX Dispenser, Liquid Medication
Regulation
21 CFR 880.6430
Device class
Class I
Review panel
General Hospital
Applicant
Burron Medical Products, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KYX

Trailing 12 months

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

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