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FDA 510(k)

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS

K-Number: K905235 · 1991-05-03

ApplicantPercussionaire Corp.
Decision Date1991-05-03
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS is the device name listed in this FDA 510(k) record. The listed applicant is Percussionaire Corp.. It received FDA 510(k) clearance on 1991-05-03 under 510(k) number K905235. 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 VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS?

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS is a medical device that received FDA 510(k) clearance on 1991-05-03. The listed applicant is Percussionaire Corp.. The 510(k) number is K905235.

When did VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS receive FDA 510(k) clearance?

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS received FDA 510(k) clearance on 1991-05-03, under 510(k) number K905235.

Who is the listed applicant for VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS?

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 VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS?

The FDA product code for VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS is CBK.

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Other records listing Percussionaire Corp. as applicant

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.

K905234TXP TRANSPORTER FAMILY AND RELATED ACCESSORIESK905236IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIESK900314PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MINK900315PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MINK900313PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MINK896586RATE INCREASE FOR IPPB/IPV

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Related Devices (Code: CBK)

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.

K253647Evita (V800); Evita (V600)Draegerwerk AG & CO KgaaK252663Inbentus VersatileIconic Solutions by Murcia, SLK251888VPAP 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.

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