Suction Catheter

FDA 510(k) K981910 · Ni-Med, Inc.

Substantially Equivalent

510(k) numberK981910

Submission

Device name
Suction Catheter
Applicant
Ni-Med, Inc.
Farmington, MO, US
Received
June 1, 1998
Decision date
August 24, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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
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
K955645Cath-GuideBSY · Traditional Hudson Respiratory Care, Inc.03/12/1996SE

More from Hudson Respiratory Care, Inc.

510(k)DeviceDecision
K875315I.V. Start KitsLRS · Traditional 02/17/1988SESD
K872824P. Urine Meter, 250CCKNX · Traditional 10/14/1987SE

Questions and answers

When was Suction Catheter cleared by the FDA?

Suction Catheter (K981910) received a 510(k) decision of Substantially Equivalent on August 24, 1998, 84 days after the submission was received.

What is the product code of K981910?

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