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FDA 510(k)

SLIMB SINGLE LIMB BREATHING CIRCUIT

K-Number: K832453 · 1983-10-27

ApplicantRespiratory Care, Inc.
Decision Date1983-10-27
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SLIMB SINGLE LIMB BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Care, Inc.. It received FDA 510(k) clearance on 1983-10-27 under 510(k) number K832453. 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 SLIMB SINGLE LIMB BREATHING CIRCUIT?

SLIMB SINGLE LIMB BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K832453.

When did SLIMB SINGLE LIMB BREATHING CIRCUIT receive FDA 510(k) clearance?

SLIMB SINGLE LIMB BREATHING CIRCUIT received FDA 510(k) clearance on 1983-10-27, under 510(k) number K832453.

Who is the listed applicant for SLIMB SINGLE LIMB BREATHING CIRCUIT?

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

What is the FDA product code for SLIMB SINGLE LIMB BREATHING CIRCUIT?

The FDA product code for SLIMB SINGLE LIMB BREATHING CIRCUIT is CAI.

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Other records listing Respiratory Care, 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.

K892230RCI VIRAL/BACTERIAL FILTERK884150MODIFIED CONCHATHERM III CONTROLLED HEATERK881625CONCHATHERM III PLUS DUAL HEAT WIRE SERVO CONTROLLK864147AQUAVALVEK863955COLBY LEVEL ALARMK861555CIRCAPAK UNIVERSAL VOLUME VENTILATOR CIRCUIT

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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

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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