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FDA 510(k)

DEKNATEL TROCAR CATHETER

K-Number: K873525 · 1987-11-02

ApplicantDeknatel, Inc.
Decision Date1987-11-02
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DEKNATEL TROCAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Deknatel, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873525. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEKNATEL TROCAR CATHETER?

DEKNATEL TROCAR 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 K873525.

When did DEKNATEL TROCAR CATHETER receive FDA 510(k) clearance?

DEKNATEL TROCAR CATHETER received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873525.

Who is the listed applicant for DEKNATEL TROCAR 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 TROCAR CATHETER?

The FDA product code for DEKNATEL TROCAR CATHETER is JOL.

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Other records listing Deknatel, Inc. as applicant

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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.

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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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