Pennine Link Yankauers

FDA 510(k) K844874 · Pennine Medical , Ltd.

Substantially Equivalent

510(k) numberK844874

Submission

Device name
Pennine Link Yankauers
Applicant
Pennine Medical , Ltd.
Derby, GB
Received
December 17, 1984
Decision date
June 6, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GEA – Cannula, Surgical, General & Plastic Surgery
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

Other 510(k)s with product code GEA

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K003965MRI Safe InstrumentsGEA · Traditional Aesculap, Inc.03/16/2001SE
K982472Genicon TrocarGEA · Traditional Genicon, LC02/04/1999SE
K954599Conmed Trogard Electronic Trocar SystemGEA · Traditional Conmedcorp11/27/1995SE
K922460Origin Secondary Cannula and TrocarGEA · Traditional Origin Medsystems, Inc.09/16/1992SE
K920110Endopath Disposable Thoracic Trocar SleeveGEA · Traditional ETHICON, Inc.04/02/1992SE
K911262Disposable Specimen Bag W/Cannula and IntroducerGEA · Traditional ETHICON, Inc.06/20/1991SE
K904881Disposable Yankauer Suction TubeGEA · Traditional Pilling Medical S.A.03/06/1991SE
K903416Cannula, SurgicalGEA · Traditional Advantage Diagnostics Corp.11/23/1990SE
K904218Suction SystemGEA · Traditional Axiom Medical, Inc.10/31/1990SE
K901718Klein Lamprey-Cannula(Tm)GEA · Traditional Jeff Klein Surgical, Inc.05/24/1990SE

More from Jeff Klein Surgical, Inc.

510(k)DeviceDecision
K854443O'Neil Urinary Catheter IntroducerKOD · Traditional 01/08/1986SE
K852859Pennine Connecting Tubing · Traditional 07/30/1985SE
K852081Pennine Oxygen Link TubingBYX · Traditional 06/14/1985SE
K844876Pennine Nelaton Catheters Sizes 5,6,8,10,12,14,16,GBX · Traditional 06/05/1985SE
K852080Pennine Suction CathetersBSY · Traditional 06/03/1985SE
K852079Pennine Derby YankauerBSY · Traditional 06/03/1985SE
K844873Pennine Guedel Airway 00,0,1,2,3 & 4CAE · Traditional 02/21/1985SE

Questions and answers

When was Pennine Link Yankauers cleared by the FDA?

Pennine Link Yankauers (K844874) received a 510(k) decision of Substantially Equivalent on June 6, 1985, 171 days after the submission was received.

What is the product code of K844874?

The FDA product code is GEA – Cannula, Surgical, General & Plastic Surgery, a Class I (low risk) device regulated under 21 CFR 878.4800.