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Hp Viridia Multi-Measurement Server/Compact Portable Patient Monitor (M3000A +3… - Rel.b

by Hewlett-Packard GmbH 510(k)

Active United States Open recall (shared submission)

510(k) K993383

Regulatory status

as of 28 Oct 2026

Recall ongoing. 1 ongoing FDA recall on shared 510(k) K993383: the recalled product is another device cleared under the same submission. See recalls

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Abbreviated NumberK993383 Date3 Feb 2000ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

2 recalls · 1 ongoing · FDA

    • Ongoing Z-1722-2025 FDA Class II initiated 7 Apr 2025 on shared 510(k) K993383

    Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.

    • Terminated Z-2531-2020 FDA Class II initiated 8 Jun 2020

    Affected M3015A extensions are incompatible with the lntelliVue X3 Patient Monitor (Model No. 867030) and lntelliVue MMX multi-measurement server (Model No. 867036).If they are connected to a host monitor, communication with the X3 or MMX could be disrupted, resulting in a loss of monitoring on the host monitor.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Specification

510(k)

510(k) Number
FDA Product Code
DSI
Models / Variants
Rel.b
Device Class
Class II
Regulation
21 CFR Part 870.1025
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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