Product code BXQ— Anesthesiology

FDA has cleared 12 devices under product code BXQ between 1984 and 2022, filed by 11 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20221 clearance
• 20171 clearance
• 20022 clearances
• 20001 clearance
• 19981 clearance
• 19931 clearance
• 19902 clearances
• 19852 clearances
• 19841 clearance

• Rhino Metrics A/S2 clearances
• Sleep Group Solutions1 clearance
• Pacificmd Biotech, LLC1 clearance
• Life-Tech Intl., Inc.1 clearance
• Jedmed Instrument Co.1 clearance
• Intertronic, Inc.1 clearance
• Hood Laboratories1 clearance
• G.M. Instruments , Ltd.1 clearance
• E. Benson Hood Lab, Inc.1 clearance
• Center Laboratories, Inc.1 clearance

• K221892 — VISIONAIRPacificmd Biotech, LLC·2022-10-05
• K170071 — SGS ECCOVISIONTM Pharyngometer, SGS ECCOVISIONTM Rhinometer, SGS ECCOVISIONTM Rhino/PharyngometerSleep Group Solutions·2017-11-09
• K022311 — RHINOSTREAM RHINOMANOMETER MODULERhino Metrics A/S·2002-10-04
• K011329 — ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETERE. Benson Hood Lab, Inc.·2002-07-26
• K000406 — RHINOSCAN MODEL SRE2000/ SRE2100 WITH ACOUSTIC RHINOMETRY MODULERhino Metrics A/S·2000-04-17
• K972140 — A1 ACOUSTIC RHINOMETERG.M. Instruments , Ltd.·1998-09-30
• K921452 — ACOUSTIC RHINOMETERHood Laboratories·1993-07-08
• K902120 — MERCURY RHINOMANOMETERLife-Tech Intl., Inc.·1990-08-06
• K896263 — RHINOMANOMETERJedmed Instrument Co.·1990-04-16
• K853024 — RHINOTEST MPIntertronic, Inc.·1985-09-27
• K851143 — RHINOMANOMETERS NR3, NR4And/Or Corp.·1985-05-23
• K844230 — RHINOMANOMETER A440 DIGITALCenter Laboratories, Inc.·1984-11-27