510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780296Substantially Equivalent

Therapy Scooter

Convaid Product Development, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780296 is the FDA 510(k) clearance record for THERAPY SCOOTER, a class I device, cleared for Convaid Product Development on under FDA product code KNL (Board, Scooter, Prone). FDA records list one 510(k) clearance for Convaid Product Development. As of , FDA records show no recalls naming K780296.

Clearance record

Decision date
Received
(3 days to decision)
Product code
KNL Board, Scooter, Prone
Regulation
21 CFR 890.5370
Device class
Class I
Review panel
Physical Medicine
Applicant
Convaid Product Development 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KNL

Trailing 12 months

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

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