FDA 510(k)

BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265

K-Number: K010265 · 2001-04-09

Decision Date2001-04-09

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265 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 2001-04-09 under 510(k) number K010265. 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 BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265?

BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265 is a medical device that received FDA 510(k) clearance on 2001-04-09. The listed applicant is Baylis Medical Co., Inc.. The 510(k) number is K010265.

When did BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265 receive FDA 510(k) clearance?

BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265 received FDA 510(k) clearance on 2001-04-09, under 510(k) number K010265.

Who is the listed applicant for BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265?

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 BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265?

The FDA product code for BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265 is GEI.

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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.