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FDA 510(k)

BITESTICK BLOCK

K-Number: K840789 · 1984-04-05

ApplicantCherry Plastics, Inc.
Decision Date1984-04-05
Product CodeJXL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BITESTICK BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Cherry Plastics, Inc.. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K840789. 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 BITESTICK BLOCK?

BITESTICK BLOCK is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Cherry Plastics, Inc.. The 510(k) number is K840789.

When did BITESTICK BLOCK receive FDA 510(k) clearance?

BITESTICK BLOCK received FDA 510(k) clearance on 1984-04-05, under 510(k) number K840789.

Who is the listed applicant for BITESTICK BLOCK?

The FDA 510(k) record lists Cherry Plastics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BITESTICK BLOCK?

The FDA product code for BITESTICK BLOCK is JXL.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cherry Plastics, Inc. 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.

K840790UNIVERSAL OXYGEN TUBING CONNECTOR

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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