FDA 510(k)

ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX

K-Number: K954229 · 1995-11-20

Decision Date1995-11-20

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1995-11-20 under 510(k) number K954229. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX?

ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX is a medical device that received FDA 510(k) clearance on 1995-11-20. The listed applicant is Valleylab, Inc.. The 510(k) number is K954229.

When did ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX receive FDA 510(k) clearance?

ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX received FDA 510(k) clearance on 1995-11-20, under 510(k) number K954229.

Who is the listed applicant for ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX?

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

What is the FDA product code for ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX?

The FDA product code for ARGON ACCESSORY WITH BLADE & NEEDLE ELECTRODE, ADAPTER BOX is GEI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.