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FDA 510(k)

VENTLAB NASAL CPAP CANNULA

K-Number: K040726 · 2004-06-03

ApplicantVentlab Corp.
Decision Date2004-06-03
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTLAB NASAL CPAP CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 2004-06-03 under 510(k) number K040726. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTLAB NASAL CPAP CANNULA?

VENTLAB NASAL CPAP CANNULA is a medical device that received FDA 510(k) clearance on 2004-06-03. The listed applicant is Ventlab Corp.. The 510(k) number is K040726.

When did VENTLAB NASAL CPAP CANNULA receive FDA 510(k) clearance?

VENTLAB NASAL CPAP CANNULA received FDA 510(k) clearance on 2004-06-03, under 510(k) number K040726.

Who is the listed applicant for VENTLAB NASAL CPAP CANNULA?

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

What is the FDA product code for VENTLAB NASAL CPAP CANNULA?

The FDA product code for VENTLAB NASAL CPAP CANNULA is BZD.

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Other records listing Ventlab 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.

K120118VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETERK102674CUFF SENTRYK093617VENTLAB 6000 SERIES HUMIDIFIERK093525ACE/STATCHECK II CO2 INDICATOR, ACE/STATCHECK II CO2 INDICATOR ARM ASSEMBY ADULT STATCHECK RESUSCITATOR WITH ACE/STATCHEK090840VENTLAB 5000 SERIES NEBULIZER ASSEMBLY, CUP, CUP W/ MASK, CUP W/ FITSALL CONN.K082204SERIES SY DISPOSABLE ELECTROSURGICAL PAD

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Related Devices (Code: BZD)

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.

K261262Altis Full Face MaskRespironics, Inc.K253044RXiBreeze PAP System (RXiBreeze 20C)Resvent Medical Technology Co., Ltd.K253553OrionResmed CorpK254104ResScan EssentialsResmed CorpK251920Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face MaskDcstar, Inc.K253166F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical 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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