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FDA 510(k)

PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI

K-Number: K896697 · 1990-02-08

Decision Date1990-02-08
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI is the device name listed in this FDA 510(k) record. The listed applicant is Deknatel, Inc.. It received FDA 510(k) clearance on 1990-02-08 under 510(k) number K896697. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI?

PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI is a medical device that received FDA 510(k) clearance on 1990-02-08. The listed applicant is Deknatel, Inc.. The 510(k) number is K896697.

When did PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI receive FDA 510(k) clearance?

PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI received FDA 510(k) clearance on 1990-02-08, under 510(k) number K896697.

Who is the listed applicant for PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI?

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 PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI?

The FDA product code for PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI is KDQ.

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.

View all 37 devices →

Related Devices (Code: KDQ)

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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