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)

UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC

K-Number: K843282 · 1984-10-22

ApplicantRush Hampton Industries
Decision Date1984-10-22
Product CodeBWH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC is the device name listed in this FDA 510(k) record. The listed applicant is Rush Hampton Industries. It received FDA 510(k) clearance on 1984-10-22 under 510(k) number K843282. The device is classified under product code BWH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC?

UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC is a medical device that received FDA 510(k) clearance on 1984-10-22. The listed applicant is Rush Hampton Industries. The 510(k) number is K843282.

When did UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC receive FDA 510(k) clearance?

UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC received FDA 510(k) clearance on 1984-10-22, under 510(k) number K843282.

Who is the listed applicant for UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC?

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

What is the FDA product code for UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC?

The FDA product code for UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC is BWH.

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: BWH)

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.

K252921Radial Jaw 4 Pulmonary Biopsy ForcepsBoston Scientific CorporationK121186RADIAL JAW 4 PULMONARY BIOPSY FORCEPSBoston Scientific CorpK102336RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS; RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS WITH NEBoston Scientific CorporationK022398REUSABLE BRONCHIAL BIOPSY FORCEPSBallard Medical ProductsK930419WILTEK BIOPSY FORCEPSWiltek Medical, 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.

↑