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FDA 510(k)

NETOH ENDOTRACHEAL TUBE HOLDER

K-Number: K940448 · 1994-02-22

Decision Date1994-02-22
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NETOH ENDOTRACHEAL TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Accessory Services, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K940448. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NETOH ENDOTRACHEAL TUBE HOLDER?

NETOH ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Medical Accessory Services, Inc.. The 510(k) number is K940448.

When did NETOH ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?

NETOH ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1994-02-22, under 510(k) number K940448.

Who is the listed applicant for NETOH ENDOTRACHEAL TUBE HOLDER?

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

What is the FDA product code for NETOH ENDOTRACHEAL TUBE HOLDER?

The FDA product code for NETOH ENDOTRACHEAL TUBE HOLDER is CBH.

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: CBH)

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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