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Solar 9500 Information Monitor

by General Electric Medical Systems Information Techn

510(k) K990068

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

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 · Traditional NumberK990068 Date14 Jul 1999ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-0524-2019 FDA Class II initiated 31 Aug 2018

    The patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time.

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  • Withdrawn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
MHX
Device Class
Class II
Regulation
21 CFR Part 870.1025
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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