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FDA 510(k)

RATE INCREASE FOR IPPB/IPV

K-Number: K896586 · 1990-01-09

ApplicantPercussionaire Corp.
Decision Date1990-01-09
Product CodeDZD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RATE INCREASE FOR IPPB/IPV is the device name listed in this FDA 510(k) record. The listed applicant is Percussionaire Corp.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K896586. The device is classified under product code DZD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RATE INCREASE FOR IPPB/IPV?

RATE INCREASE FOR IPPB/IPV is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is Percussionaire Corp.. The 510(k) number is K896586.

When did RATE INCREASE FOR IPPB/IPV receive FDA 510(k) clearance?

RATE INCREASE FOR IPPB/IPV received FDA 510(k) clearance on 1990-01-09, under 510(k) number K896586.

Who is the listed applicant for RATE INCREASE FOR IPPB/IPV?

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 RATE INCREASE FOR IPPB/IPV?

The FDA product code for RATE INCREASE FOR IPPB/IPV is DZD.

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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 ACCESSORIESK905235VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESSK905236IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIESK900314PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MINK900315PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MINK900313PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN

View all 11 devices →

Related Devices (Code: DZD)

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.

K943421ORTHODONITC ELASTOMERIC SLEEVINGJon-Ko Products, Inc.K936243REGENCY TUBEOrtho SpecialtiesK935143DENTAURUM STAINLESS STEEL TUBINGDentauraum, Inc.K911399NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)Aequitron Medical, Inc.K834446ALEXOTEK LINGUAL TUBESAlexotek Co.K834392LABIAL CUSPID TUBEAlexotek Co.

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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