FDA 510(k)

PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B

K-Number: K021778 · 2002-07-17

Decision Date2002-07-17

Product CodeDQA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2002-07-17 under 510(k) number K021778. 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 COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B?

PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B is a medical device that received FDA 510(k) clearance on 2002-07-17. The listed applicant is Philips Medical Systems. The 510(k) number is K021778.

When did PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B receive FDA 510(k) clearance?

PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B received FDA 510(k) clearance on 2002-07-17, under 510(k) number K021778.

Who is the listed applicant for PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B?

The FDA 510(k) record lists Philips Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B?

The FDA product code for PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.04, MODEL #M1275B is DQA.

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Other records listing Philips Medical Systems as applicant

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Related Devices (Code: 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.