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FDA 510(k)

HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE

K-Number: K952530 · 1995-07-24

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1995-07-24
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1995-07-24 under 510(k) number K952530. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE?

HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE is a medical device that received FDA 510(k) clearance on 1995-07-24. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K952530.

When did HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE receive FDA 510(k) clearance?

HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE received FDA 510(k) clearance on 1995-07-24, under 510(k) number K952530.

Who is the listed applicant for HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE?

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

What is the FDA product code for HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE?

The FDA product code for HEAD/NECK VASCULAR PHASED ARRAY COIL PACKAGE is LNH.

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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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