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FDA 510(k)

CONNECTORS AND AIRWAY EXTENSIONS

K-Number: K940889 · 1994-11-10

ApplicantCleveland Tubing, Inc.
Decision Date1994-11-10
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONNECTORS AND AIRWAY EXTENSIONS is the device name listed in this FDA 510(k) record. The listed applicant is Cleveland Tubing, Inc.. It received FDA 510(k) clearance on 1994-11-10 under 510(k) number K940889. 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 CONNECTORS AND AIRWAY EXTENSIONS?

CONNECTORS AND AIRWAY EXTENSIONS is a medical device that received FDA 510(k) clearance on 1994-11-10. The listed applicant is Cleveland Tubing, Inc.. The 510(k) number is K940889.

When did CONNECTORS AND AIRWAY EXTENSIONS receive FDA 510(k) clearance?

CONNECTORS AND AIRWAY EXTENSIONS received FDA 510(k) clearance on 1994-11-10, under 510(k) number K940889.

Who is the listed applicant for CONNECTORS AND AIRWAY EXTENSIONS?

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

What is the FDA product code for CONNECTORS AND AIRWAY EXTENSIONS?

The FDA product code for CONNECTORS AND AIRWAY EXTENSIONS 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 Cleveland Tubing, 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.

K945314CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBINGK940890CORRUGATED TUBINGK932119CLEVELAND TUBING, INC. VENTILATOR HOSES

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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