510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K001923Substantially Equivalent

Regency Power Wheelchair, Model 7200, 7500 & 7800

Gendron, Inc., Archbold OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001923 is the FDA 510(k) clearance record for REGENCY POWER WHEELCHAIR, MODEL 7200, 7500 & 7800, a class II device, cleared for Gendron, Inc. on under FDA product code ITI (Wheelchair, Powered). FDA's definition for product code ITI reads: "A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position” to...". FDA records list one 510(k) clearance for Gendron, Inc. As of , FDA records show no recalls naming K001923.

Clearance record

Decision date
Received
(63 days to decision)
Product code
ITI Wheelchair, Powered
Regulation
21 CFR 890.3860
Device class
Class II
Review panel
Physical Medicine
Applicant
Gendron, Inc. 400 E. Lugbill Rd., Archbold OH
510(k) summary
Summary
Third party review
No

Clearances, product code ITI

Trailing 12 months
37 clearances under product code ITI in the twelve months to October 2026, March 2026 the highest month at 7.
Show the numbers
Monthly 510(k) clearances under FDA product code ITI, trailing twelve months
MonthClearances
November 20253
December 20253
January 20262
February 20263
March 20267
April 20263
May 20261
June 20266
July 20263
August 20261
September 20265
October 20260