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FDA 510(k)

WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR

K-Number: K091516 · 2009-10-16

Decision Date2009-10-16
Product CodeEZL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Well Lead Medical Co., Ltd.. It received FDA 510(k) clearance on 2009-10-16 under 510(k) number K091516. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR?

WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR is a medical device that received FDA 510(k) clearance on 2009-10-16. The listed applicant is Well Lead Medical Co., Ltd.. The 510(k) number is K091516.

When did WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR receive FDA 510(k) clearance?

WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR received FDA 510(k) clearance on 2009-10-16, under 510(k) number K091516.

Who is the listed applicant for WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR?

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

What is the FDA product code for WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR?

The FDA product code for WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR is EZL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Well Lead Medical Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 14 devices →

Related Devices (Code: EZL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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