510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K954593Substantially Equivalent

The Aircel System

Marcon Group, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K954593 is the FDA 510(k) clearance record for THE AIRCEL SYSTEM, a class II device, cleared for Marcon Group, Inc. on under FDA product code FNM (Mattress, Air Flotation, Alternating Pressure). FDA records list one 510(k) clearance for Marcon Group, Inc. As of , FDA records show no recalls naming K954593.

Clearance record

Decision date
Received
(126 days to decision)
Product code
FNM Mattress, Air Flotation, Alternating Pressure
Regulation
21 CFR 880.5550
Device class
Class II
Review panel
General Hospital
Applicant
Marcon Group, Inc. 2000 M St., NW, Washington DC
510(k) summary
Statement
Third party review
No

Clearances, product code FNM

Trailing 12 months

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

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