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FDA 510(k)

FISK ARM SUPPORT

K-Number: K931876 · 1993-09-09

ApplicantVvortex International Corp.
Decision Date1993-09-09
Product CodeFWW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FISK ARM SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is Vvortex International Corp.. It received FDA 510(k) clearance on 1993-09-09 under 510(k) number K931876. The device is classified under product code FWW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISK ARM SUPPORT?

FISK ARM SUPPORT is a medical device that received FDA 510(k) clearance on 1993-09-09. The listed applicant is Vvortex International Corp.. The 510(k) number is K931876.

When did FISK ARM SUPPORT receive FDA 510(k) clearance?

FISK ARM SUPPORT received FDA 510(k) clearance on 1993-09-09, under 510(k) number K931876.

Who is the listed applicant for FISK ARM SUPPORT?

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

What is the FDA product code for FISK ARM SUPPORT?

The FDA product code for FISK ARM SUPPORT is FWW.

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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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