Compact Spacer

FDA 510(k) K922187 · Glaxo, Inc.

Substantially Equivalent

510(k) numberK922187

Submission

Device name
Compact Spacer
Applicant
Glaxo, Inc.
Research Triangle, NC, US
Received
May 11, 1992
Decision date
November 20, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAF – Nebulizer (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5630
Specialty
Anesthesiology

Other 510(k)s with product code CAF

510(k)DeviceApplicantDecision
K260270FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)CAF · Traditional FindAir Sp. z o.o.06/02/2026SE
K251572eRapid with eTrack SystemCAF · Traditional Pari Respiratory Equipment, Inc.12/19/2025SE
K251659Mesh Nebulizer (H6)CAF · Traditional Qingdao Future Medical Technology Co., Ltd.11/14/2025SE
K244035Portable mesh nebulizer (JM821)CAF · Traditional Shenzhen Jermei Medical Device Technology Co.…09/19/2025SE
K243468Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer…CAF · Traditional Joytech Healthcare Co. , Ltd.07/02/2025SE
K250022HeroTracker SenseCAF · Traditional Voluntis06/30/2025SE
K250583AdheResp Smart Breath-actuated Mesh NebulizerCAF · Traditional Hcmed Innovations Co., Ltd.06/20/2025SE
K242354AllNEBCAF · Traditional Enchant Tek Co. , Ltd.04/29/2025SE
K233553MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI AdapterCAF · Special Thayer Medical Corporation06/18/2024SE
K232507Aerogen®Solo Nebulizer SystemCAF · Traditional Aerogen, Ltd.05/10/2024SE

More from Aerogen, Ltd.

510(k)DeviceDecision
K954041G.R.E.E.N. Disposal Container (Note: G.R.E.E.N. Is an Acronym for Glaxo Retrieval Effort…FMI · Traditional 10/16/1995SE
K901803Syringe Needle IntroducerKZH · Traditional 11/20/1990SE
K844169VolumaticKCD · Traditional 11/09/1984SE

Questions and answers

When was Compact Spacer cleared by the FDA?

Compact Spacer (K922187) received a 510(k) decision of Substantially Equivalent on November 20, 1992, 193 days after the submission was received.

What is the product code of K922187?

The FDA product code is CAF – Nebulizer (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5630.