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)

DISPOS-A-SCOPE

K-Number: K993738 · 2000-01-06

ApplicantDispos-A-Scope
Decision Date2000-01-06
Product CodeFER
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOS-A-SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Dispos-A-Scope. It received FDA 510(k) clearance on 2000-01-06 under 510(k) number K993738. The device is classified under product code FER. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOS-A-SCOPE?

DISPOS-A-SCOPE is a medical device that received FDA 510(k) clearance on 2000-01-06. The listed applicant is Dispos-A-Scope. The 510(k) number is K993738.

When did DISPOS-A-SCOPE receive FDA 510(k) clearance?

DISPOS-A-SCOPE received FDA 510(k) clearance on 2000-01-06, under 510(k) number K993738.

Who is the listed applicant for DISPOS-A-SCOPE?

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

What is the FDA product code for DISPOS-A-SCOPE?

The FDA product code for DISPOS-A-SCOPE is FER.

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

Related Devices (Code: FER)

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.

K250645SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002)Haemoband Surgical, Ltd.K242668Gastro Concepts Air AssistGastro Concepts, LLCK230439WellCare AnoscopeWell Care (Wuhan) Medical Technology Co., Ltd.K200021Applied Medical AnoscopeApplied Medical ResourcesK171701GelPOINT Path Transanal Access PlatformApplied Medical Resources Corp.K133687THD N-ANO ANOSCOPEThd Spa

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.

↑