Nebulizer Pump Powered Models 020 and 050

FDA 510(k) K883132 · Travelneb, Inc.

Substantially Equivalent

510(k) numberK883132

Submission

Device name
Nebulizer Pump Powered Models 020 and 050
Applicant
Travelneb, Inc.
Englewood, CO, US
Received
July 26, 1988
Decision date
October 18, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTI – Compressor, Air, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.6250
Specialty
Anesthesiology

Other 510(k)s with product code BTI

510(k)DeviceApplicantDecision
K131881Ombra Table Top CompressorBTI · Traditional Trudell Medical Intl.10/24/2013SE
K113338Medical Air CompressorBTI · Traditional Oricare, Inc.08/10/2012SE
K091871DK50 DSBTI · Special Ekom S.R.O.10/23/2009SE
K072634Emg Triton -Comp,Model NCA01-XXX SeriesBTI · Traditional Emg Technology Co., Ltd.11/19/2008SE
K060781Medical Compressor, Models DK50 D and DMBTI · Traditional Ekom S.R.O.10/03/2006SE
K051691Minimate CompressorBTI · Traditional Precision Medical, Inc.12/09/2005SE
K041781Ventilair II Medical Air CompressorBTI · Traditional Hamilton Medical AG03/14/2005SE
K041406Newport C250 Air Compressor Model C250BTI · Traditional Newport Medical Instruments12/15/2004SE
K041974MED2000 Nebulizer Compressor, Models P3, P4, P5 with NebulizerBTI · Special Med2000 S.R.L.08/24/2004SE
K040220Medical Air CompressorBTI · Traditional eVent Medical, Ltd.06/09/2004SE

Questions and answers

When was Nebulizer Pump Powered Models 020 and 050 cleared by the FDA?

Nebulizer Pump Powered Models 020 and 050 (K883132) received a 510(k) decision of Substantially Equivalent on October 18, 1988, 84 days after the submission was received.

What is the product code of K883132?

The FDA product code is BTI – Compressor, Air, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.6250.