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FDA 510(k)

DUAL VALVED RESPIRATORY T

K-Number: K932781 · 1994-01-24

ApplicantInnovations For Mechanical Ventilation, Inc.
Decision Date1994-01-24
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DUAL VALVED RESPIRATORY T is the device name listed in this FDA 510(k) record. The listed applicant is Innovations For Mechanical Ventilation, Inc.. It received FDA 510(k) clearance on 1994-01-24 under 510(k) number K932781. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL VALVED RESPIRATORY T?

DUAL VALVED RESPIRATORY T is a medical device that received FDA 510(k) clearance on 1994-01-24. The listed applicant is Innovations For Mechanical Ventilation, Inc.. The 510(k) number is K932781.

When did DUAL VALVED RESPIRATORY T receive FDA 510(k) clearance?

DUAL VALVED RESPIRATORY T received FDA 510(k) clearance on 1994-01-24, under 510(k) number K932781.

Who is the listed applicant for DUAL VALVED RESPIRATORY T?

The FDA 510(k) record lists Innovations For Mechanical Ventilation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUAL VALVED RESPIRATORY T?

The FDA product code for DUAL VALVED RESPIRATORY T is CAI.

Related Clinical Trials

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.

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Other records listing Innovations For Mechanical Ventilation, Inc. 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.

K932780MALE/MALE LUER TRANSFER TUBINGK923800PRESSURE GAUGE

Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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