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FDA 510(k)

VIDEOSCAN (TM)

K-Number: K871479 · 1987-05-22

ApplicantKera Corp.
Decision Date1987-05-22
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VIDEOSCAN (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Kera Corp.. It received FDA 510(k) clearance on 1987-05-22 under 510(k) number K871479. The device is classified under product code HLQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEOSCAN (TM)?

VIDEOSCAN (TM) is a medical device that received FDA 510(k) clearance on 1987-05-22. The listed applicant is Kera Corp.. The 510(k) number is K871479.

When did VIDEOSCAN (TM) receive FDA 510(k) clearance?

VIDEOSCAN (TM) received FDA 510(k) clearance on 1987-05-22, under 510(k) number K871479.

Who is the listed applicant for VIDEOSCAN (TM)?

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

What is the FDA product code for VIDEOSCAN (TM)?

The FDA product code for VIDEOSCAN (TM) is HLQ.

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 Kera Corp. 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.

K901009MODEL 2000 INTRAOPERATIVE CORNEASCOPEK864037KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZERK850665CORNEASCOPE MODEL 1200

Related Devices (Code: HLQ)

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.

K003299OPD-SCAN, MODELS ARK-10000 AND ARK-9000Nidek Co., Ltd.K973756EYE SYS VISTAEyesys Technologies, Inc.K964290EYECHEKReichert Ophthalmic Instruments, Div. Leica, Inc.K945382TECHNOMED C-SCAN COLOR ELLIPSOID TOPOMETERExpertech Assoc., Inc.K944207TOPOGRAPHIC MODELING SYSTEM 2 TMS-2Computed Anatomy, Inc.K944616KERATRON CORNEAL TOPOGRAPHERAlliance Medical Marketinig

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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