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)

RITE-ANGLE DISPOSABLE PROPHY ANGLES

K-Number: K954802 · 1995-11-08

ApplicantAsh-USA
Decision Date1995-11-08
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RITE-ANGLE DISPOSABLE PROPHY ANGLES is the device name listed in this FDA 510(k) record. The listed applicant is Ash-USA. It received FDA 510(k) clearance on 1995-11-08 under 510(k) number K954802. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RITE-ANGLE DISPOSABLE PROPHY ANGLES?

RITE-ANGLE DISPOSABLE PROPHY ANGLES is a medical device that received FDA 510(k) clearance on 1995-11-08. The listed applicant is Ash-USA. The 510(k) number is K954802.

When did RITE-ANGLE DISPOSABLE PROPHY ANGLES receive FDA 510(k) clearance?

RITE-ANGLE DISPOSABLE PROPHY ANGLES received FDA 510(k) clearance on 1995-11-08, under 510(k) number K954802.

Who is the listed applicant for RITE-ANGLE DISPOSABLE PROPHY ANGLES?

The FDA 510(k) record lists Ash-USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RITE-ANGLE DISPOSABLE PROPHY ANGLES?

The FDA product code for RITE-ANGLE DISPOSABLE PROPHY ANGLES is EGS.

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

Related Devices (Code: EGS)

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.

K251869Disposable Prophy Angle (3399-60, 3399-090, 3399-105)Premium Plus (Dongguan) LimitedK240950Disposable Prophy AnglePacific Care LimitedK240183Star E900 Handpiece SeriesDentalez, Inc., Stardental DivisionK230106General Cutting StraightNakanishi, Inc.K222518FX ContraNakanishi, Inc.K220874Smooth Drive contra angle and straight handpiecesLares Research

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.

↑