510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K900416Substantially Equivalent

Hand Controls, Model 3700 and 3500 Series

Mobility Products & Design, Plymouth MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900416 is the FDA 510(k) clearance record for HAND CONTROLS, MODEL 3700 AND 3500 SERIES, cleared for Mobility Products & Design on under FDA product code IPQ. FDA records list one 510(k) clearance for Mobility Products & Design. As of , FDA records show no recalls naming K900416.

Clearance record

Decision date
Received
(120 days to decision)
Product code
IPQ
Review panel
Unknown
Applicant
Mobility Products & Design 14800 28th Ave. N., Plymouth MN
Third party review
No

Clearances, product code IPQ

Trailing 12 months

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

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