Disposable Specimen Bag W/Cannula and Introducer

FDA 510(k) K911262 · ETHICON, Inc.

Substantially Equivalent

510(k) numberK911262

Submission

Device name
Disposable Specimen Bag W/Cannula and Introducer
Applicant
ETHICON, Inc.
Somerville, NJ, US
Received
March 22, 1991
Decision date
June 20, 1991
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

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K003965MRI Safe InstrumentsGEA · Traditional Aesculap, Inc.03/16/2001SE
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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
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
K901717Klein Micro-Cannula(Tm)GEA · Traditional Jeff Klein Surgical, Inc.05/24/1990SE

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Questions and answers

When was Disposable Specimen Bag W/Cannula and Introducer cleared by the FDA?

Disposable Specimen Bag W/Cannula and Introducer (K911262) received a 510(k) decision of Substantially Equivalent on June 20, 1991, 90 days after the submission was received.

What is the product code of K911262?

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