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Intellivue Cl Respiration Pod

by Philips Medizinsysteme Boeblingen GmbH, Cardiac AN

510(k) K132320

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

Overview

For the INTELLIVUE CL RESPIRATION POD, this medical device directory entry provides an overview of its critical features, regulatory compliance, and user-focused support. The device is designed for adult patients undergoing anesthesia, offering a reliable and accurate respiratory monitoring system. Its compact design and intuitive interface make it easily integrated into various healthcare settings.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK132320 Date26 Mar 2014ClearedStatusActive

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  • Withdrawn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
BZQ
Device Class
Class II
Regulation
21 CFR Part 868.2375
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

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