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FDA 510(k)

BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6

K-Number: K053082 · 2005-11-30

ApplicantBaylis Medical Co., Inc.
Decision Date2005-11-30
Product CodeGXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6 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 2005-11-30 under 510(k) number K053082. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6?

BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6 is a medical device that received FDA 510(k) clearance on 2005-11-30. The listed applicant is Baylis Medical Co., Inc.. The 510(k) number is K053082.

When did BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6 receive FDA 510(k) clearance?

BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6 received FDA 510(k) clearance on 2005-11-30, under 510(k) number K053082.

Who is the listed applicant for BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6?

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 PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6?

The FDA product code for BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6 is GXI.

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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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