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FDA 510(k)

ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE

K-Number: K905450 · 1991-07-01

Decision Date1991-07-01
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1991-07-01 under 510(k) number K905450. 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 ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE?

ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE is a medical device that received FDA 510(k) clearance on 1991-07-01. The listed applicant is Vital Signs, Inc.. The 510(k) number is K905450.

When did ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE receive FDA 510(k) clearance?

ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE received FDA 510(k) clearance on 1991-07-01, under 510(k) number K905450.

Who is the listed applicant for ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE?

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

What is the FDA product code for ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE?

The FDA product code for ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE 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.

Other records listing Vital Signs, 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.

View all 75 devices →

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.

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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