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FDA 510(k)

INNERVISION,INC. LAPAROSCOPIC ELECTRODES

K-Number: K940750 · 1994-08-23

ApplicantInnervision, Inc.
Decision Date1994-08-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INNERVISION,INC. LAPAROSCOPIC ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Innervision, Inc.. It received FDA 510(k) clearance on 1994-08-23 under 510(k) number K940750. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNERVISION,INC. LAPAROSCOPIC ELECTRODES?

INNERVISION,INC. LAPAROSCOPIC ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Innervision, Inc.. The 510(k) number is K940750.

When did INNERVISION,INC. LAPAROSCOPIC ELECTRODES receive FDA 510(k) clearance?

INNERVISION,INC. LAPAROSCOPIC ELECTRODES received FDA 510(k) clearance on 1994-08-23, under 510(k) number K940750.

Who is the listed applicant for INNERVISION,INC. LAPAROSCOPIC ELECTRODES?

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

What is the FDA product code for INNERVISION,INC. LAPAROSCOPIC ELECTRODES?

The FDA product code for INNERVISION,INC. LAPAROSCOPIC ELECTRODES is GEI.

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 Innervision, 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.

K992345CHRISTOUDIAS SLIM TIP ELECTRODE INSERTK991877MACMED PAEDIATRIC INTRAMEDULLARY NAILK982428CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT)K940731INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPESK940718INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS

Related Devices (Code: GEI)

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.

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

Official Source

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