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FDA 510(k)

LIBAN INTUBATOR

K-Number: K861026 · 1986-07-28

Decision Date1986-07-28
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIBAN INTUBATOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Support Devices Co.. It received FDA 510(k) clearance on 1986-07-28 under 510(k) number K861026. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBAN INTUBATOR?

LIBAN INTUBATOR is a medical device that received FDA 510(k) clearance on 1986-07-28. The listed applicant is Life Support Devices Co.. The 510(k) number is K861026.

When did LIBAN INTUBATOR receive FDA 510(k) clearance?

LIBAN INTUBATOR received FDA 510(k) clearance on 1986-07-28, under 510(k) number K861026.

Who is the listed applicant for LIBAN INTUBATOR?

The FDA 510(k) record lists Life Support Devices Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIBAN INTUBATOR?

The FDA product code for LIBAN INTUBATOR is CCW.

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.

Related Devices (Code: CCW)

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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