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)

JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS

K-Number: K103726 · 2012-02-08

ApplicantIntegra LifeSciences Corporation
Decision Date2012-02-08
Product CodeKNF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Integra LifeSciences Corporation. It received FDA 510(k) clearance on 2012-02-08 under 510(k) number K103726. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS?

JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2012-02-08. The listed applicant is Integra LifeSciences Corporation. The 510(k) number is K103726.

When did JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS received FDA 510(k) clearance on 2012-02-08, under 510(k) number K103726.

Who is the listed applicant for JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS?

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

What is the FDA product code for JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS?

The FDA product code for JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS is KNF.

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 Integra LifeSciences Corporation 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.

K251162CUSA® Clarity Ultrasonic Surgical Aspirator SystemK250752AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)K240493CUSA® Clarity Ultrasonic Surgical Aspirator SystemK230427CUSA Clarity Ultrasonic Surgical Aspirator SystemK221835CUSA Clarity Ultrasonic Surgical Aspirator SystemK221763CUSA Clarity Ultrasonic Surgical Aspirator System

View all 56 devices →

Related Devices (Code: KNF)

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.

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KGK250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, 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.

↑