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FDA 510(k)

RF TUNNELER WIRE

K-Number: K051670 · 2006-03-30

ApplicantBaylis Medical Co., Inc.
Decision Date2006-03-30
Product CodePDU
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RF TUNNELER WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Co., Inc.. It received FDA 510(k) clearance on 2006-03-30 under 510(k) number K051670. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RF TUNNELER WIRE?

RF TUNNELER WIRE is a medical device that received FDA 510(k) clearance on 2006-03-30. The listed applicant is Baylis Medical Co., Inc.. The 510(k) number is K051670.

When did RF TUNNELER WIRE receive FDA 510(k) clearance?

RF TUNNELER WIRE received FDA 510(k) clearance on 2006-03-30, under 510(k) number K051670.

Who is the listed applicant for RF TUNNELER WIRE?

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

What is the FDA product code for RF TUNNELER WIRE?

The FDA product code for RF TUNNELER WIRE is PDU.

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Other records listing Baylis Medical Co., Inc. as applicant

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Related Devices (Code: PDU)

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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.

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