510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923977Substantially Equivalent

Akrotech 4000

Lumex, Inc., Bay Shore NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923977 is the FDA 510(k) clearance record for AKROTECH 4000, a class II device, cleared for Lumex, Inc. on under FDA product code IOQ (Bed, Flotation Therapy, Powered). FDA records list 8 510(k) clearances for Lumex, Inc., from to . As of , FDA records show no recalls naming K923977.

Clearance record

Decision date
Received
(189 days to decision)
Product code
IOQ Bed, Flotation Therapy, Powered
Regulation
21 CFR 890.5170
Device class
Class II
Review panel
Physical Medicine
Applicant
Lumex, Inc. 100 Spence St., Bay Shore NY
510(k) summary
Statement
Third party review
No

Clearances, product code IOQ

Trailing 12 months

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

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