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FDA 510(k)

HOOD NASAL SPLINT

K-Number: K890599 · 1989-03-17

ApplicantHood Laboratories
Decision Date1989-03-17
Product CodeEPP
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HOOD NASAL SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Hood Laboratories. It received FDA 510(k) clearance on 1989-03-17 under 510(k) number K890599. The device is classified under product code EPP. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOD NASAL SPLINT?

HOOD NASAL SPLINT is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Hood Laboratories. The 510(k) number is K890599.

When did HOOD NASAL SPLINT receive FDA 510(k) clearance?

HOOD NASAL SPLINT received FDA 510(k) clearance on 1989-03-17, under 510(k) number K890599.

Who is the listed applicant for HOOD NASAL SPLINT?

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 HOOD NASAL SPLINT?

The FDA product code for HOOD NASAL SPLINT is EPP.

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Other records listing Hood Laboratories as applicant

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.

K921452ACOUSTIC RHINOMETERK920994HOOD NASAL SEPTAL BUTTONK905703KRUPIN EYE VALVE WITH DISKK904821ELIACHAR MODIFIED ESOPHAGEAL STENTK897049GIBSON ENDOLYMPHATIC SHUNTK897059HOOD SPEAKING VALVE

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Related Devices (Code: EPP)

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.

K942158AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITSWfr/Aquaplast Corp.K942724EXTERNAL NASAL SPLINTMicromed Development Corp.K895502MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINTMicrobio-Medics, Inc.K882244RICHARDS THERMOPLASTIC DORSAL NASAL SPLINTRichards Medical Co., Inc.K872905AMERICAN NASAL SPONGEAmerican Silk Sutures, Inc.K864932'EXMOOR' CAWOOD NASAL SPLINTSExmoor Plastics , Ltd.

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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