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FDA 510(k)

CYBERRX MODEL 7200

K-Number: K934434 · 1995-01-24

ApplicantCybermed Control Systems, Inc.
Decision Date1995-01-24
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CYBERRX MODEL 7200 is the device name listed in this FDA 510(k) record. The listed applicant is Cybermed Control Systems, Inc.. It received FDA 510(k) clearance on 1995-01-24 under 510(k) number K934434. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYBERRX MODEL 7200?

CYBERRX MODEL 7200 is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Cybermed Control Systems, Inc.. The 510(k) number is K934434.

When did CYBERRX MODEL 7200 receive FDA 510(k) clearance?

CYBERRX MODEL 7200 received FDA 510(k) clearance on 1995-01-24, under 510(k) number K934434.

Who is the listed applicant for CYBERRX MODEL 7200?

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

What is the FDA product code for CYBERRX MODEL 7200?

The FDA product code for CYBERRX MODEL 7200 is FFT.

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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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