Nebu-Sol Metered Dose Dispenser (TM)

FDA 510(k) K910239 · Dey Laboratories, Inc.

Substantially Equivalent

510(k) numberK910239

Submission

Device name
Nebu-Sol Metered Dose Dispenser (TM)
Applicant
Dey Laboratories, Inc.
Napa, CA, US
Received
January 22, 1991
Decision date
May 22, 1991
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.

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K875024Dey-Pak and Dey-Vial Sodium Chloride Solution, UspCCQ · Traditional 01/22/1988SE
K875011Dey-Pak Purified Water, Usp, SterileCCQ · Traditional 01/22/1988SE
K831532Ocular Irrigating CannulaHMX · Traditional 07/12/1983SE

Questions and answers

When was Nebu-Sol Metered Dose Dispenser (TM) cleared by the FDA?

Nebu-Sol Metered Dose Dispenser (TM) (K910239) received a 510(k) decision of Substantially Equivalent on May 22, 1991, 120 days after the submission was received.

What is the product code of K910239?

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