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FDA 510(k)

JOHNSON INTRATRACHEAL OXYGEN CATHETER SET

K-Number: K870181 · 1987-05-14

ApplicantCook, Inc.
Decision Date1987-05-14
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

JOHNSON INTRATRACHEAL OXYGEN CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1987-05-14 under 510(k) number K870181. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNSON INTRATRACHEAL OXYGEN CATHETER SET?

JOHNSON INTRATRACHEAL OXYGEN CATHETER SET is a medical device that received FDA 510(k) clearance on 1987-05-14. The listed applicant is Cook, Inc.. The 510(k) number is K870181.

When did JOHNSON INTRATRACHEAL OXYGEN CATHETER SET receive FDA 510(k) clearance?

JOHNSON INTRATRACHEAL OXYGEN CATHETER SET received FDA 510(k) clearance on 1987-05-14, under 510(k) number K870181.

Who is the listed applicant for JOHNSON INTRATRACHEAL OXYGEN CATHETER SET?

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

What is the FDA product code for JOHNSON INTRATRACHEAL OXYGEN CATHETER SET?

The FDA product code for JOHNSON INTRATRACHEAL OXYGEN CATHETER SET is BTO.

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Other records listing Cook, Inc. as applicant

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Related Devices (Code: BTO)

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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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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