FDA 510(k)

PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN

K-Number: K900313 · 1990-10-26

Decision Date1990-10-26

Product CodeCBK

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN is the device name listed in this FDA 510(k) record. The listed applicant is Percussionaire Corp.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K900313. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN?

PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Percussionaire Corp.. The 510(k) number is K900313.

When did PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN receive FDA 510(k) clearance?

PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN received FDA 510(k) clearance on 1990-10-26, under 510(k) number K900313.

Who is the listed applicant for PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN?

The FDA 510(k) record lists Percussionaire Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN?

The FDA product code for PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN is CBK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Percussionaire Corp. as applicant

K905234TXP TRANSPORTER FAMILY AND RELATED ACCESSORIES K905235VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS K905236IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES K900314PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN K900315PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MIN K896586RATE INCREASE FOR IPPB/IPV

View all 11 devices →

Related Devices (Code: CBK)

K253647Evita (V800); Evita (V600)Draegerwerk AG & CO Kgaa K252663Inbentus VersatileIconic Solutions by Murcia, SL K251888VPAP Pediatric Face MaskHsiner Co., Ltd.K232365Vivo 45 LSOconnell Regulatory Consultants, Inc.K252173F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size A (ONIV117A); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size B (ONIV117B); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size C (ONIV117C); F&P OptiNIV ONIV117-F Hospital Vented Full Face Mask with optional Expiratory Filter Compatible with Single-limb Circuits - Size A (ONIV117A-F); F&P OptiNIV ONIV117-F Hospital Vented FullFisher & Paykel Healthcare, Ltd.K243767SV600, SV800 VentilatorShenzhen Mindray Bio-Medical Electronics Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.