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FDA 510(k)

JACKSON BITE BLOCKS

K-Number: K822018 · 1982-08-03

ApplicantKelleher Corp.
Decision Date1982-08-03
Product CodeJXL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

JACKSON BITE BLOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-03 under 510(k) number K822018. The device is classified under product code JXL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACKSON BITE BLOCKS?

JACKSON BITE BLOCKS is a medical device that received FDA 510(k) clearance on 1982-08-03. The listed applicant is Kelleher Corp.. The 510(k) number is K822018.

When did JACKSON BITE BLOCKS receive FDA 510(k) clearance?

JACKSON BITE BLOCKS received FDA 510(k) clearance on 1982-08-03, under 510(k) number K822018.

Who is the listed applicant for JACKSON BITE BLOCKS?

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

What is the FDA product code for JACKSON BITE BLOCKS?

The FDA product code for JACKSON BITE BLOCKS is JXL.

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Other records listing Kelleher Corp. 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.

K822618EMERGENCY TRACHEOSTOMY INSTRUMENT SETK822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPHK823083ELECTROSURGICAL UNITK822252ENT TREATMENT UNITSK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS

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Related Devices (Code: JXL)

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.

K221469PATI (Protector Against Tongue Injury)Neurovice, LLCK201309ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size MediumMecta CorporationK172978SurgeoBiteSurgovations, LLCK050188EPIGUARDEpisafe Medical Devices, Ltd.K992269VENTIL-A ORAL PROTECTORSomatics, Inc.K960663UNIVERSAL BITE BLOCKB&B Medical Technologies, Inc.

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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