PLEUR-EVAC-A-7000--ADULT/PEDI Chest Drainage Syst

FDA 510(k) K882223 · Deknatel, Inc.

Substantially Equivalent

510(k) numberK882223

Submission

Device name
PLEUR-EVAC-A-7000--ADULT/PEDI Chest Drainage Syst
Applicant
Deknatel, Inc.
Lake Success, NY, US
Received
May 26, 1988
Decision date
August 16, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KDQ – Bottle, Collection, Vacuum
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6740
Specialty
General Hospital

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K962856Pleur-Evac Sahara Adult/Pediatric Chest Drainage System Model S-1100, S-1200, 2-2100…KDQ · Traditional Deknatel, Inc.08/28/1996SE
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K962168Mucus Specimen TrapKDQ · Traditional Sage Products, Inc.07/22/1996SE
K950677Atrium Dry Suction Control Water Seal Chest DrainKDQ · Traditional Atrium Medical Corp.04/13/1995SE
K941818PM9000 Vac TrapKDQ · Traditional Precision Medical, Inc.12/12/1994SE
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More from Davol, Inc.

510(k)DeviceDecision
K963850Pleur-Evac Sahara Plus Model S-1150 Continuous Reinfusion Autotransfusion SystemCAC · Traditional 04/22/1997SE
K962683Snowden-Pencer Computerized High Flow InsufflatorHIF · Traditional 01/10/1997SE
K964070Deknatel DSP Pleur-Evac Autotransfusion Blood Recovery BagCAC · Traditional 12/31/1996SE
K963098Pleur-Evac Shara Plus Model S-2150/CONTINUOUS Reinfusion Autotransfusion SYSTEM(S-100)CAC · Traditional 11/08/1996SE
K962856Pleur-Evac Sahara Adult/Pediatric Chest Drainage System Model S-1100, S-1200, 2-2100…KDQ · Traditional 08/28/1996SE
K925243Deknatel(Tm) Pleur-Evac(R) Thoracic CatheterGBX · Traditional 07/27/1994SE
K930740Surgical Suture, Nonabsorable Stainless SteelGAQ · Traditional 07/26/1994SE
K930739Sutures Polyprop., Polyetheline, Nylon & SilkGAP · Traditional 07/26/1994SE
K930738Surgical Sutures, PGL, Gut, Deklene, Opthamend EtcGAL · Traditional 07/26/1994SE
K926338Pleur-Evac Cardiotomy Reservoir # CR-9400 & 9400FCAC · Traditional 07/26/1994SE

Questions and answers

When was PLEUR-EVAC-A-7000--ADULT/PEDI Chest Drainage Syst cleared by the FDA?

PLEUR-EVAC-A-7000--ADULT/PEDI Chest Drainage Syst (K882223) received a 510(k) decision of Substantially Equivalent on August 16, 1988, 82 days after the submission was received.

What is the product code of K882223?

The FDA product code is KDQ – Bottle, Collection, Vacuum, a Class II (moderate risk) device regulated under 21 CFR 880.6740.