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)

ULTRAGUIDE 1000

K-Number: K974432 · 1998-02-09

ApplicantUltraguide , Ltd.
Decision Date1998-02-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRAGUIDE 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Ultraguide , Ltd.. It received FDA 510(k) clearance on 1998-02-09 under 510(k) number K974432. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAGUIDE 1000?

ULTRAGUIDE 1000 is a medical device that received FDA 510(k) clearance on 1998-02-09. The listed applicant is Ultraguide , Ltd.. The 510(k) number is K974432.

When did ULTRAGUIDE 1000 receive FDA 510(k) clearance?

ULTRAGUIDE 1000 received FDA 510(k) clearance on 1998-02-09, under 510(k) number K974432.

Who is the listed applicant for ULTRAGUIDE 1000?

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

What is the FDA product code for ULTRAGUIDE 1000?

The FDA product code for ULTRAGUIDE 1000 is IYO.

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 Ultraguide , Ltd. 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.

K023227USG 2000SAK022354ULTRAGUIDE CTG 2000SAK013150MR-GUIDE 2000K011418ULTRAGUIDE MR-GUIDE 3000K002258ULTRAGUIDE CT-GUIDE 1010

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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.

↑