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FDA 510(k)

DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC

K-Number: K831344 · 1983-07-18

ApplicantBrimms, Inc.
Decision Date1983-07-18
Product Code
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC is the device name listed in this FDA 510(k) record. The listed applicant is Brimms, Inc.. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K831344. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC?

DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Brimms, Inc.. The 510(k) number is K831344.

When did DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC receive FDA 510(k) clearance?

DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831344.

Who is the listed applicant for DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC?

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

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.

K842788DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE

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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