DEKNATEL THORACIC CATHETER
K-Number: K873517 · 1987-11-02
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Device Summary
Frequently Asked Questions
What is the DEKNATEL THORACIC CATHETER?
DEKNATEL THORACIC CATHETER is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Deknatel, Inc.. The 510(k) number is K873517.
When did DEKNATEL THORACIC CATHETER receive FDA 510(k) clearance?
DEKNATEL THORACIC CATHETER received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873517.
Who is the listed applicant for DEKNATEL THORACIC CATHETER?
The FDA 510(k) record lists Deknatel, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEKNATEL THORACIC CATHETER?
The FDA product code for DEKNATEL THORACIC CATHETER is JOL.
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 Deknatel, Inc. 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.
Related Devices (Code: JOL)
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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