FDA 510(k)

BIRD (VDR) SINUSOIDAL PERCUSSIONATORS

K-Number: K895486 · 1989-10-13

Decision Date1989-10-13

Product CodeCBK

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

BIRD (VDR) SINUSOIDAL PERCUSSIONATORS is the device name listed in this FDA 510(k) record. The listed applicant is Percussionaire Corp.. It received FDA 510(k) clearance on 1989-10-13 under 510(k) number K895486. 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 BIRD (VDR) SINUSOIDAL PERCUSSIONATORS?

BIRD (VDR) SINUSOIDAL PERCUSSIONATORS is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Percussionaire Corp.. The 510(k) number is K895486.

When did BIRD (VDR) SINUSOIDAL PERCUSSIONATORS receive FDA 510(k) clearance?

BIRD (VDR) SINUSOIDAL PERCUSSIONATORS received FDA 510(k) clearance on 1989-10-13, under 510(k) number K895486.

Who is the listed applicant for BIRD (VDR) SINUSOIDAL PERCUSSIONATORS?

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 BIRD (VDR) SINUSOIDAL PERCUSSIONATORS?

The FDA product code for BIRD (VDR) SINUSOIDAL PERCUSSIONATORS is CBK.

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Other records listing Percussionaire Corp. as applicant

K905234TXP TRANSPORTER FAMILY AND RELATED ACCESSORIES K905235VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS K905236IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES K900313PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN K900315PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MIN K900314PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN

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Related Devices (Code: CBK)

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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.