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FDA 510(k)

CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY

K-Number: K901279 · 1990-03-28

ApplicantChatham Industries
Decision Date1990-03-28
Product CodeBTQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Chatham Industries. It received FDA 510(k) clearance on 1990-03-28 under 510(k) number K901279. The device is classified under product code BTQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY?

CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY is a medical device that received FDA 510(k) clearance on 1990-03-28. The listed applicant is Chatham Industries. The 510(k) number is K901279.

When did CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY receive FDA 510(k) clearance?

CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY received FDA 510(k) clearance on 1990-03-28, under 510(k) number K901279.

Who is the listed applicant for CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY?

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

What is the FDA product code for CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY?

The FDA product code for CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY is BTQ.

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Related Devices (Code: BTQ)

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.

K940320AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGSAd-Tech Medical Instrument CorpK921353NASOPHARYNGEAL AIRWAYCoast Medical Corp.K911784NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAYNorth American Sterilization & Packaging Co.K903618ROBERTAZZI NASOPHARYNGEAL AIRWAYEastmed Enterprises, Inc.K900456POLAMEDCO NASOPAHARYNGEAL AIRWAYPolamedco, Inc.K883668SUNDERLAND NASAL TUBEExmoor Plastics , Ltd.

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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