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)

ESYS SYSTEM

K-Number: K933492 · 1994-03-25

ApplicantEndolap, Inc.
Decision Date1994-03-25
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ESYS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Endolap, Inc.. It received FDA 510(k) clearance on 1994-03-25 under 510(k) number K933492. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESYS SYSTEM?

ESYS SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-25. The listed applicant is Endolap, Inc.. The 510(k) number is K933492.

When did ESYS SYSTEM receive FDA 510(k) clearance?

ESYS SYSTEM received FDA 510(k) clearance on 1994-03-25, under 510(k) number K933492.

Who is the listed applicant for ESYS SYSTEM?

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

What is the FDA product code for ESYS SYSTEM?

The FDA product code for ESYS SYSTEM is HET.

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 Endolap, 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.

K974516ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODEK974515ENDOLAP RESECTOSCOPE ROLLER ELECTRODEK950243TITAN INSUFFLATION NEEDLEK950219ENDOLAP INSUFFLATOR TUBING SET

Related Devices (Code: HET)

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.

K250939SIRIUS Endoscope System (PR-SI-1230)Precision Robotics (Hong Kong) LimitedK243821i-CutA.M.I. Agency For Medical Innovations GmbHK221642SIRIUS Endoscope SystemPrecision Robotics (Hong Kong) LimitedK210116Video Endoscopy System, 3D Video Endoscopy SystemSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.K201832Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5Olympus Medical Systems Corp.K210104SurroundScope System270surgical , Ltd.

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.

↑