510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050425Substantially Equivalent

Aura-Psg

Astro-Med, Inc., West Warwick RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K050425 is the FDA 510(k) clearance record for AURA-PSG, a class II device, cleared for Astro-Med, Inc. on under FDA product code OLV (Standard Polysomnograph With Electroencephalograph). FDA's definition for product code OLV reads: "Acquire, display, store, and archive electroencephalographic signals from the brain and other signals (such as electromyography, respiratory and/or oximetry signals) for sleep recordings. May also be used to allow on-screen review...". FDA records list 13 510(k) clearances for Astro-Med, Inc., from to . As of , FDA records show no recalls naming K050425.

Clearance record

Decision date
Received
(244 days to decision)
Product code
OLV Standard Polysomnograph With Electroencephalograph
Regulation
21 CFR 882.1400
Device class
Class II
Review panel
Neurology
Applicant
Astro-Med, Inc. 600 E. Greenwich Ave., West Warwick RI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OLV

Trailing 12 months
2 clearances under product code OLV in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code OLV, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260