Frazier Suction Instrument-Dispos

FDA 510(k) K832636 · Pilling Co.

Substantially Equivalent

510(k) numberK832636

Submission

Device name
Frazier Suction Instrument-Dispos
Applicant
Pilling Co.
Mchenry, IL, US
Received
August 4, 1983
Decision date
October 14, 1983
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
K002582Pilling E-Frazier Bipolar Suction TubeGEI · Traditional 11/03/2000SE
K934427Pilling Laparoscopic InstrumentationGEI · Traditional 01/10/1994SE
K925370Triangular Jaw Microlaryngeal ForcepsELW · Traditional 03/18/1993SE
K925198Kaiser No Cannula Thoracoscopy/Laparoscopy InstrGCJ · Traditional 02/12/1993SE
K922971No-Scalpel Vascetomy InstrumentsKOA · Traditional 09/23/1992SE
K914015Clement-Pilling Cholangiography Cath Guide/ClampGBZ · Traditional 11/21/1991SE
K911099Mehigan-Pilling Angioscopic Vascular Instrum. LineDWX · Traditional 06/25/1991SE
K911100Mehigan-Pilling Phlebetome TMMGZ · Traditional 06/21/1991SE
K904507Pilling Brush ValvulotomeDWQ · Traditional 03/01/1991SE
K884946Jehle Coronary Perfusion CathetersKRA · Traditional 02/06/1989SE

Questions and answers

When was Frazier Suction Instrument-Dispos cleared by the FDA?

Frazier Suction Instrument-Dispos (K832636) received a 510(k) decision of Substantially Equivalent on October 14, 1983, 71 days after the submission was received.

What is the product code of K832636?

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