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FDA 510(k)

HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST

K-Number: K920199 · 1992-03-06

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1992-03-06
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST 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 1992-03-06 under 510(k) number K920199. 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 COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST?

HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST is a medical device that received FDA 510(k) clearance on 1992-03-06. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K920199.

When did HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST receive FDA 510(k) clearance?

HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST received FDA 510(k) clearance on 1992-03-06, under 510(k) number K920199.

Who is the listed applicant for HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST?

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 COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST?

The FDA product code for HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST 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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