FDA 510(k)

PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A.

K-Number: K052377 · 2005-11-17

ApplicantPhilips Medizin Systeme Boeblingen GmbH

Decision Date2005-11-17

Product CodeDQA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A. is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. It received FDA 510(k) clearance on 2005-11-17 under 510(k) number K052377. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A.?

PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A. is a medical device that received FDA 510(k) clearance on 2005-11-17. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K052377.

When did PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A. receive FDA 510(k) clearance?

PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A. received FDA 510(k) clearance on 2005-11-17, under 510(k) number K052377.

Who is the listed applicant for PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A.?

The FDA 510(k) record lists Philips Medizin Systeme Boeblingen GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A.?

The FDA product code for PHILIPS DISPOSABLE SPO2 SENSORS MII32A AND M1133A. is DQA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.