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)

CONMED VCARE RETRACTOR/ELEVATOR

K-Number: K955446 · 1996-06-18

ApplicantConmedcorp
Decision Date1996-06-18
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONMED VCARE RETRACTOR/ELEVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-06-18 under 510(k) number K955446. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED VCARE RETRACTOR/ELEVATOR?

CONMED VCARE RETRACTOR/ELEVATOR is a medical device that received FDA 510(k) clearance on 1996-06-18. The listed applicant is Conmedcorp. The 510(k) number is K955446.

When did CONMED VCARE RETRACTOR/ELEVATOR receive FDA 510(k) clearance?

CONMED VCARE RETRACTOR/ELEVATOR received FDA 510(k) clearance on 1996-06-18, under 510(k) number K955446.

Who is the listed applicant for CONMED VCARE RETRACTOR/ELEVATOR?

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

What is the FDA product code for CONMED VCARE RETRACTOR/ELEVATOR?

The FDA product code for CONMED VCARE RETRACTOR/ELEVATOR is LKF.

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 Conmedcorp 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.

K101534CONMED ALTRUS THERMAL TISSUE FUSION SYSTEMK061021ENTAKE STANDARD AND SAFETY PEG SYSTEMK050992CONMED IRRIGATION NOZZLEK050777PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907K050304FX WIRE ADVANCED MEASUREMENT GUIDEWIREK041953VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART

View all 92 devices →

Related Devices (Code: LKF)

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.

K253403FemVue® Controlled Saline-Air Device (FSA-300)Femasys, Inc.K252260RELIEEV HSG Catheter (HSG7FA1)Li Medical Corporation , Ltd.K242002FemVue MINI Saline-Air DeviceFemasys, Inc.K240364RELIEEV Uterine Manipulator Injector (CUMI 5.0)Li Medical Corporation , Ltd.K241693FemChec Controlled Saline-Air Device (FCD-250)Femasys, Inc.K222798Rejoni Intrauterine CatheterRejoni, 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.

↑