Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE

K-Number: K842788 · 1984-09-11

ApplicantBrimms, Inc.
Decision Date1984-09-11
Product CodeJXL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Brimms, Inc.. It received FDA 510(k) clearance on 1984-09-11 under 510(k) number K842788. 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 DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE?

DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is Brimms, Inc.. The 510(k) number is K842788.

When did DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE receive FDA 510(k) clearance?

DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842788.

Who is the listed applicant for DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE?

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

What is the FDA product code for DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE?

The FDA product code for DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE 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 Brimms, 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.

K831344DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC

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.

↑