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)

USI DENTAL POLISHER. A/G-20

K-Number: K873147 · 1987-10-14

ApplicantCranston Ind., Inc.
Decision Date1987-10-14
Product CodeEFA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

USI DENTAL POLISHER. A/G-20 is the device name listed in this FDA 510(k) record. The listed applicant is Cranston Ind., Inc.. It received FDA 510(k) clearance on 1987-10-14 under 510(k) number K873147. The device is classified under product code EFA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USI DENTAL POLISHER. A/G-20?

USI DENTAL POLISHER. A/G-20 is a medical device that received FDA 510(k) clearance on 1987-10-14. The listed applicant is Cranston Ind., Inc.. The 510(k) number is K873147.

When did USI DENTAL POLISHER. A/G-20 receive FDA 510(k) clearance?

USI DENTAL POLISHER. A/G-20 received FDA 510(k) clearance on 1987-10-14, under 510(k) number K873147.

Who is the listed applicant for USI DENTAL POLISHER. A/G-20?

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

What is the FDA product code for USI DENTAL POLISHER. A/G-20?

The FDA product code for USI DENTAL POLISHER. A/G-20 is EFA.

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 Cranston Ind., 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.

K873146USI BASIC. AG 1050. AG 1090

Related Devices (Code: EFA)

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.

K192809Dental HandpieceMicro-Nx Co., Ltd.K163239SMARTmaticKaltenbach & Voigt GmbHK101172RDT3 HANDPIECE HEAD MODEL RDT3Redent Nova, Ltd.K093894ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLEAnthogyrK092446INTRA LUX HEAD 3 LDSYKaltenbach & Voigt GmbH & Co.K090055LOW & HIGH SPEED KITDpm USA Corp.

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.

↑