FDA 510(k)

ACOUSTIC RHINOMETER

K-Number: K921452 · 1993-07-08

Decision Date1993-07-08

Product CodeBXQ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

ACOUSTIC RHINOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Hood Laboratories. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K921452. The device is classified under product code BXQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACOUSTIC RHINOMETER?

ACOUSTIC RHINOMETER is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Hood Laboratories. The 510(k) number is K921452.

When did ACOUSTIC RHINOMETER receive FDA 510(k) clearance?

ACOUSTIC RHINOMETER received FDA 510(k) clearance on 1993-07-08, under 510(k) number K921452.

Who is the listed applicant for ACOUSTIC RHINOMETER?

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

What is the FDA product code for ACOUSTIC RHINOMETER?

The FDA product code for ACOUSTIC RHINOMETER is BXQ.

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Other records listing Hood Laboratories as applicant

K920994HOOD NASAL SEPTAL BUTTON K905703KRUPIN EYE VALVE WITH DISK K904821ELIACHAR MODIFIED ESOPHAGEAL STENT K897049GIBSON ENDOLYMPHATIC SHUNT K897059HOOD SPEAKING VALVE K893866HOOD PEDIATRIC TRACHEOSTOMY TUBE

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Related Devices (Code: BXQ)

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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.