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)

DR.500O OPERATING TABLE

K-Number: K864295 · 1986-11-19

ApplicantKoken Mfg Company, Inc.
Decision Date1986-11-19
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DR.500O OPERATING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Koken Mfg Company, Inc.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K864295. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR.500O OPERATING TABLE?

DR.500O OPERATING TABLE is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Koken Mfg Company, Inc.. The 510(k) number is K864295.

When did DR.500O OPERATING TABLE receive FDA 510(k) clearance?

DR.500O OPERATING TABLE received FDA 510(k) clearance on 1986-11-19, under 510(k) number K864295.

Who is the listed applicant for DR.500O OPERATING TABLE?

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

What is the FDA product code for DR.500O OPERATING TABLE?

The FDA product code for DR.500O OPERATING TABLE is FQO.

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 Koken Mfg Company, 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.

K864501KOKEN'S NEW MODEL M-3000 POWER TABLEK864574MAC 150E OPTHALMIC CHAIRK864494MODEL 6500 OPTHALMIC CHAIRK864325DR7700 OPERATING TABLE

Related Devices (Code: FQO)

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.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K971307AMSCO SURGICAL TABLESTERIS Corporation

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.

↑