Skip to content

Amplifier Otrona, Model N3A-Emg

by Honeywell, Inc.

510(k) K772102

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 10 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 10 Oct 2026. What this means

Regulatory status

as of registry sync 10 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK772102 Date21 Nov 1977ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 10 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  • Withdrawn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
GWL
Device Class
Class II
Regulation
21 CFR Part 882.1835
Advisory Committee
Neurology
FDA Decision
SESE Substantially Equivalent

Other devices from Honeywell, Inc.

See all devices from Honeywell, Inc. →