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)

THREE MODELS OF TABLES, STOOLS, & LIGHTS

K-Number: K811190 · 1981-05-08

ApplicantMidmark Corp.
Decision Date1981-05-08
Product CodeLGX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THREE MODELS OF TABLES, STOOLS, & LIGHTS is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1981-05-08 under 510(k) number K811190. The device is classified under product code LGX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THREE MODELS OF TABLES, STOOLS, & LIGHTS?

THREE MODELS OF TABLES, STOOLS, & LIGHTS is a medical device that received FDA 510(k) clearance on 1981-05-08. The listed applicant is Midmark Corp.. The 510(k) number is K811190.

When did THREE MODELS OF TABLES, STOOLS, & LIGHTS receive FDA 510(k) clearance?

THREE MODELS OF TABLES, STOOLS, & LIGHTS received FDA 510(k) clearance on 1981-05-08, under 510(k) number K811190.

Who is the listed applicant for THREE MODELS OF TABLES, STOOLS, & LIGHTS?

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

What is the FDA product code for THREE MODELS OF TABLES, STOOLS, & LIGHTS?

The FDA product code for THREE MODELS OF TABLES, STOOLS, & LIGHTS is LGX.

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 Midmark Corp. 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.

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CK112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

View all 31 devices →

Related Devices (Code: LGX)

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.

K945163ECHOCARDIOGRAPHYTri W-G, Inc.K894144POWER EXAMINATION TABLE MODEL # 405Midmark Corp.K894134POWER EXAMINATION TABLE MODEL # 411Midmark Corp.K883680MEDALIST EXAMINATION TABLEHamilton Industries, Inc.K882010POWER EXAMINATION TABLEEnochs Mfg., Inc.K864072ADEC 1005-C CHAIRCherne Industries, 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.

↑