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)

E-TYPE CONTRA ANGLE NAC-E

K-Number: K962540 · 1996-09-12

ApplicantNsk Nakanishi, Inc.
Decision Date1996-09-12
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

E-TYPE CONTRA ANGLE NAC-E is the device name listed in this FDA 510(k) record. The listed applicant is Nsk Nakanishi, Inc.. It received FDA 510(k) clearance on 1996-09-12 under 510(k) number K962540. 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 E-TYPE CONTRA ANGLE NAC-E?

E-TYPE CONTRA ANGLE NAC-E is a medical device that received FDA 510(k) clearance on 1996-09-12. The listed applicant is Nsk Nakanishi, Inc.. The 510(k) number is K962540.

When did E-TYPE CONTRA ANGLE NAC-E receive FDA 510(k) clearance?

E-TYPE CONTRA ANGLE NAC-E received FDA 510(k) clearance on 1996-09-12, under 510(k) number K962540.

Who is the listed applicant for E-TYPE CONTRA ANGLE NAC-E?

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

What is the FDA product code for E-TYPE CONTRA ANGLE NAC-E?

The FDA product code for E-TYPE CONTRA ANGLE NAC-E 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

Other records listing Nsk Nakanishi, 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.

K991701MACH-SIGMA HANDPIECE, ULTRAPUSH, MODELS MACH-SIGMA MU (MINI HEAD), MACH-SIGMA SU (STD. HEAD), MACH-SIGMA TU (TORQUE HD)K991021SONIC SCALER WITH FIBER OPTIC, MODEL NAS-L, SONIC SCALER WITHOUT FIBER OPTIC, MODEL NAS-NLK990954ELEC-MATE, MODELS EX-6 SET, EX-6L SET, EX-30 SETK990682PROPHY-MATE MOTOR HANDPIECE, MODELS PROPHY-MATE (2000 RPM MAX), ENDO-MATE (600RPM MAX.)K990646PORTABLE ELECTRIC MOTOR-HANDPIECE UNIT, HANDY-MATEK980162MACH-SIGMA HANDPIECE, ULTRAPUSH

View all 13 devices →

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.

↑