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FDA 510(k)

RADIO FREQUENCY RECEIVER SUBSYSTEM

K-Number: K900725 · 1990-03-23

ApplicantMyheal Technologies
Decision Date1990-03-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIO FREQUENCY RECEIVER SUBSYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Myheal Technologies. It received FDA 510(k) clearance on 1990-03-23 under 510(k) number K900725. 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 RADIO FREQUENCY RECEIVER SUBSYSTEM?

RADIO FREQUENCY RECEIVER SUBSYSTEM is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is Myheal Technologies. The 510(k) number is K900725.

When did RADIO FREQUENCY RECEIVER SUBSYSTEM receive FDA 510(k) clearance?

RADIO FREQUENCY RECEIVER SUBSYSTEM received FDA 510(k) clearance on 1990-03-23, under 510(k) number K900725.

Who is the listed applicant for RADIO FREQUENCY RECEIVER SUBSYSTEM?

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

What is the FDA product code for RADIO FREQUENCY RECEIVER SUBSYSTEM?

The FDA product code for RADIO FREQUENCY RECEIVER SUBSYSTEM is LNH.

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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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