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FDA 510(k)

PERCUNAV SYSTEM

K-Number: K132087 · 2013-07-24

ApplicantPhilips Health Care
Decision Date2013-07-24
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PERCUNAV SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Health Care. It received FDA 510(k) clearance on 2013-07-24 under 510(k) number K132087. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUNAV SYSTEM?

PERCUNAV SYSTEM is a medical device that received FDA 510(k) clearance on 2013-07-24. The listed applicant is Philips Health Care. The 510(k) number is K132087.

When did PERCUNAV SYSTEM receive FDA 510(k) clearance?

PERCUNAV SYSTEM received FDA 510(k) clearance on 2013-07-24, under 510(k) number K132087.

Who is the listed applicant for PERCUNAV SYSTEM?

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

What is the FDA product code for PERCUNAV SYSTEM?

The FDA product code for PERCUNAV SYSTEM is JAK.

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Related Devices (Code: JAK)

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Official Source

View on FDA Database →

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

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