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FDA 510(k)

PENTAX Medical Video Upper GI Scopes (EG Family)

K-Number: K190799 · 2019-11-12

ApplicantPentax of America, Inc.
Decision Date2019-11-12
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PENTAX Medical Video Upper GI Scopes (EG Family) is a medical device manufactured by Pentax of America, Inc.. It received FDA 510(k) clearance on 2019-11-12 under approval number K190799. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX Medical Video Upper GI Scopes (EG Family)?

PENTAX Medical Video Upper GI Scopes (EG Family) is a medical device that received FDA 510(k) clearance on 2019-11-12. It is manufactured by Pentax of America, Inc.. The 510(k) number is K190799.

When was PENTAX Medical Video Upper GI Scopes (EG Family) approved by the FDA?

PENTAX Medical Video Upper GI Scopes (EG Family) received FDA 510(k) clearance on 2019-11-12, under approval number K190799.

What company makes PENTAX Medical Video Upper GI Scopes (EG Family)?

PENTAX Medical Video Upper GI Scopes (EG Family) is manufactured by Pentax of America, Inc..

What is the FDA product code for PENTAX Medical Video Upper GI Scopes (EG Family)?

The FDA product code for PENTAX Medical Video Upper GI Scopes (EG Family) is FDS.

Related Clinical Trials

NCT07027826 The Esophageal String Test as a Diagnostic Screening Tool for Eosinophilic Esophagitis Among Africans With Dysphagia in Mali and the United States RECRUITING NCT07614529 Hyperangulated vs Standard Videolaryngoscopy vs Direct Laryngoscopy for Double-Lumen Endobronchial Tube Intubation NOT_YET_RECRUITING NCT05072483 Natural History Study of CADASIL RECRUITING NCT06466161 Conical Forearm and Cylindrical Upper Arm Non-Invasive Blood Pressure (NIBP) Measurements in Pregnant Patients RECRUITING NCT07136506 Gait Analysis Parameter and Upper Limb Evaluation in Control Participants RECRUITING NCT07267689 Evaluation of a Hypertonic Seawater Aerosol Therapy Solution in Adults and Children RECRUITING

Related PubMed Literature

PMID: 39964125 Potential health benefits of lactoferrin and derived peptides - how to qualify as a medical device? Critical reviews in microbiology (2025) PMID: 39943397 Clinical Validation of a Video-Otoscopy-Based Medical Device for the Remote Diagnosis of Ear Complaints. Sensors (Basel, Switzerland) (2025)

Other Devices by Pentax of America, Inc.

K162151PENTAX Medical ENT Video Imaging System K162447PENTAX Medical Endoscopic Ultrasound System, EG-3270UK Upper G.I. Video Scope (Convex Array Type) with EPK-i5010 Video Processor and HI VISION Preirus Ultrasound Scanner K182004PENTAX Medical Endoscopic Ultrasound System K181522PENTAX MEDICAL ED-3490TK, Video Duodenoscope, PENTAX Medical ED34-i10T, Video Duodenoscope K173679PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes K173554PENTAX Medical Video Bronchoscopes, PENTAX Medical Video Naso-Pharyngo-Laryngoscope, and PENTAX Medical Ultrasond Video Bronchoscope

View all 39 devices →

Related Devices (Code: FDS)

K153206Fujifilm Ultrasonic Processors SU-1 PLATINUM and SU-1Fujifilm Medical System U.S.A., Inc. K162749FUJIFILM Hood Models DH-28GR, DH-29CR and DH-30CRFujifilm Medical Systems U.S.A, Inc. K180292PENTAX Video Upper G.I. Scope EG34-i10Pentax Medical of America, Inc. K180341FUJIFILM 600 Series Endoscope EG-600WR v2Fujifilm Corporation K181763FUJIFILM Ultrasonic EndoscopeFujifilm Corporation K180911Visura Technologies TEECAD SystemVisura Technologies, LLC

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.

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