510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843282Substantially Equivalent

Universal by Rush-Hampton Arthroscopic

Rush Hampton Industries, Sanford FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843282 is the FDA 510(k) clearance record for UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC, a class II device, cleared for Rush Hampton Industries on under FDA product code BWH (Forceps, Biopsy, Bronchoscope (Non-Rigid)). FDA's definition for product code BWH reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list one 510(k) clearance for Rush Hampton Industries. As of , FDA records show no recalls naming K843282.

Clearance record

Decision date
Received
(63 days to decision)
Product code
BWH Forceps, Biopsy, Bronchoscope (Non-Rigid)
Regulation
21 CFR 874.4680
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Rush Hampton Industries P.O. Box 5500, Sanford FL
Third party review
No

Clearances, product code BWH

Trailing 12 months

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

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