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FDA 510(k)

VIMEDIC SYSTEM TM

K-Number: K800163 · 1980-02-05

ApplicantMedical Systems Group of Viskay, Inc.
Decision Date1980-02-05
Product CodeEFA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VIMEDIC SYSTEM TM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Group of Viskay, Inc.. It received FDA 510(k) clearance on 1980-02-05 under 510(k) number K800163. The device is classified under product code EFA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIMEDIC SYSTEM TM?

VIMEDIC SYSTEM TM is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Medical Systems Group of Viskay, Inc.. The 510(k) number is K800163.

When did VIMEDIC SYSTEM TM receive FDA 510(k) clearance?

VIMEDIC SYSTEM TM received FDA 510(k) clearance on 1980-02-05, under 510(k) number K800163.

Who is the listed applicant for VIMEDIC SYSTEM TM?

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

What is the FDA product code for VIMEDIC SYSTEM TM?

The FDA product code for VIMEDIC SYSTEM TM is EFA.

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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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