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)

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC

K-Number: K925716 · 1992-12-17

ApplicantBennett X-Ray Corp.
Decision Date1992-12-17
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K925716. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC?

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K925716.

When did BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC receive FDA 510(k) clearance?

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC received FDA 510(k) clearance on 1992-12-17, under 510(k) number K925716.

Who is the listed applicant for BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC?

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

What is the FDA product code for BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC?

The FDA product code for BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC is IYB.

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 Bennett X-Ray 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.

K964576PROFILE MAMMOGRAPHY SYSTEM (M-PRO)K952672VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEMK944978BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSIK945962BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHYK945731HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORSK945749BENNETT X-RAY TOMOGRAPHY SYSTEM

View all 23 devices →

Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, 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.

↑