FDA 510(k)

NASOPHARYNGEAL AIRWAY-ROBERTAZZI

K-Number: K850644 · 1985-03-21

Decision Date1985-03-21

Product CodeBTQ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

NASOPHARYNGEAL AIRWAY-ROBERTAZZI is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1985-03-21 under 510(k) number K850644. 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 NASOPHARYNGEAL AIRWAY-ROBERTAZZI?

NASOPHARYNGEAL AIRWAY-ROBERTAZZI is a medical device that received FDA 510(k) clearance on 1985-03-21. The listed applicant is Dryden Corp.. The 510(k) number is K850644.

When did NASOPHARYNGEAL AIRWAY-ROBERTAZZI receive FDA 510(k) clearance?

NASOPHARYNGEAL AIRWAY-ROBERTAZZI received FDA 510(k) clearance on 1985-03-21, under 510(k) number K850644.

Who is the listed applicant for NASOPHARYNGEAL AIRWAY-ROBERTAZZI?

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

What is the FDA product code for NASOPHARYNGEAL AIRWAY-ROBERTAZZI?

The FDA product code for NASOPHARYNGEAL AIRWAY-ROBERTAZZI is BTQ.

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Other records listing Dryden Corp. as applicant

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Related Devices (Code: BTQ)

K940320AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGSAd-Tech Medical Instrument Corp K921353NASOPHARYNGEAL AIRWAYCoast Medical Corp.K911784NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAYNorth American Sterilization & Packaging Co.K903618ROBERTAZZI NASOPHARYNGEAL AIRWAYEastmed Enterprises, Inc.K900456POLAMEDCO NASOPAHARYNGEAL AIRWAYPolamedco, Inc.K901279CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAYChatham Industries

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.