510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931168Substantially Equivalent

X-20 Air Support Bed

American Life Support Technology, Inc., Redwood City CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931168 is the FDA 510(k) clearance record for X-20 AIR SUPPORT BED, a class II device, cleared for American Life Support Technology, Inc. on under FDA product code INX (Bed, Air Fluidized). FDA records list one 510(k) clearance for American Life Support Technology, Inc. As of , FDA records show no recalls naming K931168.

Clearance record

Decision date
Received
(346 days to decision)
Product code
INX Bed, Air Fluidized
Regulation
21 CFR 890.5160
Device class
Class II
Review panel
Physical Medicine
Applicant
American Life Support Technology, Inc. 101 Saginaw Dr., Redwood City CA
510(k) summary
Summary
Third party review
No

Clearances, product code INX

Trailing 12 months

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

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