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FDA 510(k)

CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING

K-Number: K945314 · 1994-11-18

ApplicantCleveland Tubing, Inc.
Decision Date1994-11-18
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING 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 1994-11-18 under 510(k) number K945314. 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 CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING?

CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING is a medical device that received FDA 510(k) clearance on 1994-11-18. The listed applicant is Cleveland Tubing, Inc.. The 510(k) number is K945314.

When did CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING receive FDA 510(k) clearance?

CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING received FDA 510(k) clearance on 1994-11-18, under 510(k) number K945314.

Who is the listed applicant for CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING?

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 CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING?

The FDA product code for CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K940889CONNECTORS AND AIRWAY EXTENSIONSK940890CORRUGATED 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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