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)

J SINGLE USE HEAD AND JD REUSABLE HANDLE

K-Number: K950555 · 1995-12-28

ApplicantMicro-Mega Societe Anonyme
Decision Date1995-12-28
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

J SINGLE USE HEAD AND JD REUSABLE HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Mega Societe Anonyme. It received FDA 510(k) clearance on 1995-12-28 under 510(k) number K950555. 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 J SINGLE USE HEAD AND JD REUSABLE HANDLE?

J SINGLE USE HEAD AND JD REUSABLE HANDLE is a medical device that received FDA 510(k) clearance on 1995-12-28. The listed applicant is Micro-Mega Societe Anonyme. The 510(k) number is K950555.

When did J SINGLE USE HEAD AND JD REUSABLE HANDLE receive FDA 510(k) clearance?

J SINGLE USE HEAD AND JD REUSABLE HANDLE received FDA 510(k) clearance on 1995-12-28, under 510(k) number K950555.

Who is the listed applicant for J SINGLE USE HEAD AND JD REUSABLE HANDLE?

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

What is the FDA product code for J SINGLE USE HEAD AND JD REUSABLE HANDLE?

The FDA product code for J SINGLE USE HEAD AND JD REUSABLE HANDLE 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 Societe Anonyme 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.

K103123APEX POINTER+; MEASRUING CABLE, HOOK, LIP CLIP, TOUCH PROBE (ACCESSORIES)K081268SONIC AIR MM1500 + (MID), MODEL 50400014K042171AX'S ENDO 04, 06, 08, 2.5, 40 , MODELS 50100206, 50100217, 50100218, 50100230, 50100232K971350SERIES XE, SERIES SE, SERIES TEK961275SIRIUS 10, 10L, 40, 40LK961235SIRIUS 180, 180L, 230, 230L

View all 10 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.

↑