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FDA 510(k)

DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER

K-Number: K042709 · 2005-01-18

Decision Date2005-01-18
Product CodeEZL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Tyco Healthcare. It received FDA 510(k) clearance on 2005-01-18 under 510(k) number K042709. 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 DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER?

DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER is a medical device that received FDA 510(k) clearance on 2005-01-18. The listed applicant is Tyco Healthcare. The 510(k) number is K042709.

When did DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER receive FDA 510(k) clearance?

DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER received FDA 510(k) clearance on 2005-01-18, under 510(k) number K042709.

Who is the listed applicant for DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER?

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

What is the FDA product code for DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER?

The FDA product code for DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER 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 Tyco Healthcare 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

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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