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FDA 510(k)

CLEVELAND TUBING, INC. VENTILATOR HOSES

K-Number: K932119 · 1993-06-23

Decision Date1993-06-23
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLEVELAND TUBING, INC. VENTILATOR HOSES 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 1993-06-23 under 510(k) number K932119. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEVELAND TUBING, INC. VENTILATOR HOSES?

CLEVELAND TUBING, INC. VENTILATOR HOSES is a medical device that received FDA 510(k) clearance on 1993-06-23. The listed applicant is Cleveland Tubing, Inc.. The 510(k) number is K932119.

When did CLEVELAND TUBING, INC. VENTILATOR HOSES receive FDA 510(k) clearance?

CLEVELAND TUBING, INC. VENTILATOR HOSES received FDA 510(k) clearance on 1993-06-23, under 510(k) number K932119.

Who is the listed applicant for CLEVELAND TUBING, INC. VENTILATOR HOSES?

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. VENTILATOR HOSES?

The FDA product code for CLEVELAND TUBING, INC. VENTILATOR HOSES is BZO.

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 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.

Related Devices (Code: BZO)

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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