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FDA 510(k)

KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT

K-Number: K880683 · 1988-03-09

ApplicantKing Systems Corp.
Decision Date1988-03-09
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is King Systems Corp.. It received FDA 510(k) clearance on 1988-03-09 under 510(k) number K880683. 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 KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT?

KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is King Systems Corp.. The 510(k) number is K880683.

When did KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT receive FDA 510(k) clearance?

KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT received FDA 510(k) clearance on 1988-03-09, under 510(k) number K880683.

Who is the listed applicant for KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT?

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

What is the FDA product code for KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT?

The FDA product code for KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT is CAI.

Related Clinical Trials

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Other records listing King Systems 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.

K033189KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305K033186KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205K021634KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105K012485MS-140 ALL-ROUND ENHANCED PERFORMANCE FILTER; MS-141 ALL-ROUND ENHANCED PERFORMANCE ANGLED; MS-142 ALL-ROUND/HME ENHANCEK010040SLEEVED FILTERK990614HME-BOOSTER

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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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