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)

ARTHROSCOPE

K-Number: K931792 · 1994-06-13

ApplicantIntramed Laboratories, Inc.
Decision Date1994-06-13
Product CodeHRH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Intramed Laboratories, Inc.. It received FDA 510(k) clearance on 1994-06-13 under 510(k) number K931792. The device is classified under product code HRH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPE?

ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1994-06-13. The listed applicant is Intramed Laboratories, Inc.. The 510(k) number is K931792.

When did ARTHROSCOPE receive FDA 510(k) clearance?

ARTHROSCOPE received FDA 510(k) clearance on 1994-06-13, under 510(k) number K931792.

Who is the listed applicant for ARTHROSCOPE?

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

What is the FDA product code for ARTHROSCOPE?

The FDA product code for ARTHROSCOPE is HRH.

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 Intramed Laboratories, 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.

K953258TITANIUM HEMOSTATIC CLIPK942457GRAFT THROMBECTOMY INSTRUMENTSK925283VALVULOTOMEK934696ANGIOSCOPEK922114ENDOSCOPIC RETRIEVAL BASKETK914385OPTICAL VALVULOTOME

View all 14 devices →

Related Devices (Code: HRH)

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.

K022843GAYHEART CORNEAL EXCISION DEVICEStephens InstrumentsK873918HEAD & CHIN RESTSRichmond Products, Inc.K864520BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRONPrecision Instruments, Inc.K862524DEKNATEL (R) TREPHINEDeknatel, Inc.K861825CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADEStorz Instrument Co.K860648BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIAPrecision Instruments, 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.

↑