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Msas Professional

by Biomeridian, Int.

510(k) K993824

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK993824 Date20 Jan 2000ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
GZO
Device Class
Class II
Regulation
21 CFR Part 882.1540
Advisory Committee
Neurology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 6 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Msas Professional is a device for galvanic skin response measurement. It functions as a neurology device designed to record and measure skin conductance changes.

This device is classified as a Class 2 medical device under regulation number 882.1540. It received FDA 510(k) clearance under the reference number K993824.

Other devices from Biomeridian, Int.

  • Msas-Vantage

    Class II

Questions

AI-generated answers, 6 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the MSAS Professional used for?

    The MSAS Professional is a neurology device manufactured by Biomeridian, Int. that is specifically designed to record and measure changes in skin conductance through galvanic skin response measurement.

  • How is the MSAS Professional classified?

    The device is classified as a Class 2 medical device under regulation number 882.1540, which pertains to galvanic skin response measurement devices.

  • Does this device have FDA clearance?

    Yes, the MSAS Professional received FDA 510(k) clearance under reference number K993824, which was granted on January 20, 2000.