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FDA 510(k)

PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO

K-Number: K880162 · 1988-03-21

ApplicantDeknatel, Inc.
Decision Date1988-03-21
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO is the device name listed in this FDA 510(k) record. The listed applicant is Deknatel, Inc.. It received FDA 510(k) clearance on 1988-03-21 under 510(k) number K880162. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO?

PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is Deknatel, Inc.. The 510(k) number is K880162.

When did PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO receive FDA 510(k) clearance?

PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO received FDA 510(k) clearance on 1988-03-21, under 510(k) number K880162.

Who is the listed applicant for PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO?

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--A-5002 CHEST DRAINAGE SYSTEM W/AUTO?

The FDA product code for PLEUR-EVAC--A-5002 CHEST DRAINAGE SYSTEM W/AUTO is CAC.

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Other records listing Deknatel, Inc. as applicant

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Related Devices (Code: CAC)

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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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