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FDA 510(k)

MOBILE MRP-7000

K-Number: K920159 · 1992-03-05

ApplicantHitachi Medical Systems America, Inc.
Decision Date1992-03-05
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILE MRP-7000 is the device name listed in this FDA 510(k) record. The listed applicant is Hitachi Medical Systems America, Inc.. It received FDA 510(k) clearance on 1992-03-05 under 510(k) number K920159. 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 MOBILE MRP-7000?

MOBILE MRP-7000 is a medical device that received FDA 510(k) clearance on 1992-03-05. The listed applicant is Hitachi Medical Systems America, Inc.. The 510(k) number is K920159.

When did MOBILE MRP-7000 receive FDA 510(k) clearance?

MOBILE MRP-7000 received FDA 510(k) clearance on 1992-03-05, under 510(k) number K920159.

Who is the listed applicant for MOBILE MRP-7000?

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

What is the FDA product code for MOBILE MRP-7000?

The FDA product code for MOBILE MRP-7000 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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