Catheters, Greenline Suction

FDA 510(k) K790606 · Snyder Laboratories, Inc.

Substantially Equivalent

510(k) numberK790606

Submission

Device name
Catheters, Greenline Suction
Applicant
Snyder Laboratories, Inc.
Mchenry, IL, US
Received
March 29, 1979
Decision date
April 23, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BSY – Catheters, Suction, Tracheobronchial
Device class
Class I (low risk)
Regulation
21 CFR 868.6810
Specialty
Anesthesiology

Other 510(k)s with product code BSY

510(k)DeviceApplicantDecision
K031997Mallinckrodt Dar Ty-Care / Ty-Care Exel Closed Suction SystemBSY · Traditional Mallinckrodt Dar S.R.L.11/25/2003SE
K992902Ambu Hand Power Suction PumpBSY · Traditional Ambu, Inc.10/25/1999SE
K982945Dual Purpose Closed CatheterBSY · Traditional Spirit Medical Systems, Inc.09/22/1998SE
K981910Suction CatheterBSY · Traditional Ni-Med, Inc.08/24/1998SE
K972258Hi-Care Closed Suction SystemBSY · Traditional Mallinckrodt Medical12/29/1997SE
K973199Amsino Suction CatheterBSY · Traditional Amsino Intl., Inc.09/10/1997SE
K961707Trach-Eze Closed Ventilation Suction SystemBSY · Traditional Sorenson Critical Care03/11/1997SE
K964369Trach Care Set with MicrobanBSY · Traditional Ballard Medical Products02/11/1997SE
K960488Neo 2 Line Suction SystemBSY · Traditional Alcove Medical, Inc.04/26/1996SE
K955831Argyle Aspr-Care Closed Suction SystemBSY · Traditional Sherwood Medical Co.03/28/1996SE

More from Sherwood Medical Co.

510(k)DeviceDecision
K843906Snyder Hemovac Wound Drainage DevicesGBS · Traditional 11/05/1984SE
K821321Snyder Debribement System LDP-1BTA · Traditional 08/06/1982SE
K800861Snyder Hemovac Chest Drainage SolutionKDQ · Traditional 05/02/1980SE
K800578Surgivac TMGCY · Traditional 04/16/1980SE
K800577Snyder Hemovac TM Vented Wound KitGCY · Traditional 04/16/1980SE
K800543Snyder Hysterectomy Y Tube KitGCY · Traditional 04/16/1980SE
K800542100 ML Snyder HemovacGCY · Traditional 04/02/1980SE
K790607Greenline Irrigation TraysEYN · Traditional 05/11/1979SE
K790420Suction Connecting TubingBYY · Traditional 04/23/1979SE
K790419Yankauer & Poodle Suction InstrumentsBYY · Traditional 04/23/1979SE

Questions and answers

When was Catheters, Greenline Suction cleared by the FDA?

Catheters, Greenline Suction (K790606) received a 510(k) decision of Substantially Equivalent on April 23, 1979, 25 days after the submission was received.

What is the product code of K790606?

The FDA product code is BSY – Catheters, Suction, Tracheobronchial, a Class I (low risk) device regulated under 21 CFR 868.6810.