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FDA 510(k)

CONSULTIVA REPORT STATION, MODEL RS-1

K-Number: K031248 · 2003-06-20

ApplicantMiramedica, Inc.
Decision Date2003-06-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONSULTIVA REPORT STATION, MODEL RS-1 is the device name listed in this FDA 510(k) record. The listed applicant is Miramedica, Inc.. It received FDA 510(k) clearance on 2003-06-20 under 510(k) number K031248. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSULTIVA REPORT STATION, MODEL RS-1?

CONSULTIVA REPORT STATION, MODEL RS-1 is a medical device that received FDA 510(k) clearance on 2003-06-20. The listed applicant is Miramedica, Inc.. The 510(k) number is K031248.

When did CONSULTIVA REPORT STATION, MODEL RS-1 receive FDA 510(k) clearance?

CONSULTIVA REPORT STATION, MODEL RS-1 received FDA 510(k) clearance on 2003-06-20, under 510(k) number K031248.

Who is the listed applicant for CONSULTIVA REPORT STATION, MODEL RS-1?

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

What is the FDA product code for CONSULTIVA REPORT STATION, MODEL RS-1?

The FDA product code for CONSULTIVA REPORT STATION, MODEL RS-1 is LLZ.

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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.

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