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FDA 510(k)

MEDILOG VISION

K-Number: K961636 · 1997-01-17

ApplicantOxford Instruments, Plc.
Decision Date1997-01-17
Product CodeOLZ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDILOG VISION is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Instruments, Plc.. It received FDA 510(k) clearance on 1997-01-17 under 510(k) number K961636. The device is classified under product code OLZ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG VISION?

MEDILOG VISION is a medical device that received FDA 510(k) clearance on 1997-01-17. The listed applicant is Oxford Instruments, Plc.. The 510(k) number is K961636.

When did MEDILOG VISION receive FDA 510(k) clearance?

MEDILOG VISION received FDA 510(k) clearance on 1997-01-17, under 510(k) number K961636.

Who is the listed applicant for MEDILOG VISION?

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

What is the FDA product code for MEDILOG VISION?

The FDA product code for MEDILOG VISION is OLZ.

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 Oxford Instruments, Plc. 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.

K981405SYNERGY LTK961642MEDILOG MR95K930714SONICAID MODEL TEAM FECG IUPK933816SONICAID MODEL P110 FETAL HEAR DETECTOR

Related Devices (Code: OLZ)

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.

K253390SOMNUM (SOMNUM)Honeynaps Co., Ltd.K253668Onera SleepMap (SLEEPMAP)Onera B.V.K250851Hypnos (369054-200)Cadwell Industries, Inc.K252330DeepRESPNox Medical EhfK250058NEAT 001Brain Electrophysiology Laboratory Company, LLCK241960DeepRESPNox Medical Ehf

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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