Pleur-Evac Cardiotomy Reservoir # CR-9400 & 9400F

FDA 510(k) K926338 · Deknatel, Inc.

Substantially Equivalent

510(k) numberK926338

Submission

Device name
Pleur-Evac Cardiotomy Reservoir # CR-9400 & 9400F
Applicant
Deknatel, Inc.
San Jose-Heredia, CR
Received
December 18, 1992
Decision date
July 26, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAC – Apparatus, Autotransfusion
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5830
Specialty
Anesthesiology
Life-sustaining
Yes

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More from Fresenius Kabi AG

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
K931106Biosurge(Tm) Synchronous Autotrans Procedure KitCAC · Traditional 10/06/1993SE

Questions and answers

When was Pleur-Evac Cardiotomy Reservoir # CR-9400 & 9400F cleared by the FDA?

Pleur-Evac Cardiotomy Reservoir # CR-9400 & 9400F (K926338) received a 510(k) decision of Substantially Equivalent on July 26, 1994, 585 days after the submission was received.

What is the product code of K926338?

The FDA product code is CAC – Apparatus, Autotransfusion, a Class II (moderate risk) device regulated under 21 CFR 868.5830.