510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933051Substantially Equivalent

Zero Gravity Wheelchair Components, Modification

General Components Intl., Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933051 is the FDA 510(k) clearance record for ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION, a class I device, cleared for General Components Intl., Inc. on under FDA product code KNN (Components, Wheelchair). FDA records list 2 510(k) clearances for General Components Intl., Inc., from to . As of , FDA records show no recalls naming K933051.

Clearance record

Decision date
Received
(140 days to decision)
Product code
KNN Components, Wheelchair
Regulation
21 CFR 890.3920
Device class
Class I
Review panel
Physical Medicine
Applicant
General Components Intl., Inc. 363 W. 2720 S., Suite B, Salt Lake City UT
510(k) summary
Summary
Third party review
No

Clearances, product code KNN

Trailing 12 months

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

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