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)

MID LABS TWIN ILLUMINATOR

K-Number: K932131 · 1994-04-01

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date1994-04-01
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MID LABS TWIN ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrument Development Laboratories, Inc.. It received FDA 510(k) clearance on 1994-04-01 under 510(k) number K932131. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MID LABS TWIN ILLUMINATOR?

MID LABS TWIN ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K932131.

When did MID LABS TWIN ILLUMINATOR receive FDA 510(k) clearance?

MID LABS TWIN ILLUMINATOR received FDA 510(k) clearance on 1994-04-01, under 510(k) number K932131.

Who is the listed applicant for MID LABS TWIN ILLUMINATOR?

The FDA 510(k) record lists Medical Instrument Development Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MID LABS TWIN ILLUMINATOR?

The FDA product code for MID LABS TWIN ILLUMINATOR is EQH.

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 Medical Instrument Development Laboratories, 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.

K102222ULTIMATE VIT ENHAMCER (UVE)K020911MID LABS AUTONOMOUS VIT ENHANCER (AVE)K992943VIT ENHANCERK971067DIGI-INJECTORK950287UNIVIT PROBEK934600MICRODRIVE

View all 22 devices →

Related Devices (Code: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, Inc.

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.

↑