FDA 510(k)

LITERATURE ON THE SONADENT

K-Number: K827410 · 1982-06-04

Decision Date1982-06-04

Product Code

DecisionSubstantially Equivalent

Device Summary

LITERATURE ON THE SONADENT is the device name listed in this FDA 510(k) record. The listed applicant is L&R Mfg. Co., Inc.. It received FDA 510(k) clearance on 1982-06-04 under 510(k) number K827410. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITERATURE ON THE SONADENT?

LITERATURE ON THE SONADENT is a medical device that received FDA 510(k) clearance on 1982-06-04. The listed applicant is L&R Mfg. Co., Inc.. The 510(k) number is K827410.

When did LITERATURE ON THE SONADENT receive FDA 510(k) clearance?

LITERATURE ON THE SONADENT received FDA 510(k) clearance on 1982-06-04, under 510(k) number K827410.

Who is the listed applicant for LITERATURE ON THE SONADENT?

The FDA 510(k) record lists L&R Mfg. Co., 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.