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)

IMKB CONTRA-ANGLES

K-Number: K933639 · 1994-09-21

ApplicantMicro-Mega
Decision Date1994-09-21
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMKB CONTRA-ANGLES is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Mega. It received FDA 510(k) clearance on 1994-09-21 under 510(k) number K933639. 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 IMKB CONTRA-ANGLES?

IMKB CONTRA-ANGLES is a medical device that received FDA 510(k) clearance on 1994-09-21. The listed applicant is Micro-Mega. The 510(k) number is K933639.

When did IMKB CONTRA-ANGLES receive FDA 510(k) clearance?

IMKB CONTRA-ANGLES received FDA 510(k) clearance on 1994-09-21, under 510(k) number K933639.

Who is the listed applicant for IMKB CONTRA-ANGLES?

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

What is the FDA product code for IMKB CONTRA-ANGLES?

The FDA product code for IMKB CONTRA-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

Other records listing Micro-Mega 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.

K970649HERO 642

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.

↑