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FDA 510(k)

VENTI-VOICE NASAL CATHETER

K-Number: K834522 · 1984-01-17

ApplicantRespiratory Support Products, Inc.
Decision Date1984-01-17
Product CodeESE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VENTI-VOICE NASAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1984-01-17 under 510(k) number K834522. The device is classified under product code ESE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTI-VOICE NASAL CATHETER?

VENTI-VOICE NASAL CATHETER is a medical device that received FDA 510(k) clearance on 1984-01-17. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K834522.

When did VENTI-VOICE NASAL CATHETER receive FDA 510(k) clearance?

VENTI-VOICE NASAL CATHETER received FDA 510(k) clearance on 1984-01-17, under 510(k) number K834522.

Who is the listed applicant for VENTI-VOICE NASAL CATHETER?

The FDA 510(k) record lists Respiratory Support Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTI-VOICE NASAL CATHETER?

The FDA product code for VENTI-VOICE NASAL CATHETER is ESE.

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Other records listing Respiratory Support Products, Inc. as applicant

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Related Devices (Code: ESE)

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.

K934483NU-VOIS BATTERY POWERED ARTIFICIAL LARYNXMountain Precision Mfg. Ltd. Co.K931371DENRICK SPEECH AID (DR-1)Denrick Corp.K923648LECTRO-LARYNXBruce Medical SupplyK914816AMERICAN ARTIFICIAL LARYNXUltravoice, Ltd.K901503ADDVOX BONE CONDUCTOR AMPLIFIER SPEAKER SYSTEMStanton Magnetics, Inc.K860992VOX COMPANIONBloomfield Research and Development, Inc.

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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