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FDA 510(k)

VILLAN (VIDEO LIFT LINK ANALYSIS)

K-Number: K910712 · 1991-05-21

ApplicantPhysio Systems, Inc.
Decision Date1991-05-21
Product CodeLXI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VILLAN (VIDEO LIFT LINK ANALYSIS) is the device name listed in this FDA 510(k) record. The listed applicant is Physio Systems, Inc.. It received FDA 510(k) clearance on 1991-05-21 under 510(k) number K910712. The device is classified under product code LXI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VILLAN (VIDEO LIFT LINK ANALYSIS)?

VILLAN (VIDEO LIFT LINK ANALYSIS) is a medical device that received FDA 510(k) clearance on 1991-05-21. The listed applicant is Physio Systems, Inc.. The 510(k) number is K910712.

When did VILLAN (VIDEO LIFT LINK ANALYSIS) receive FDA 510(k) clearance?

VILLAN (VIDEO LIFT LINK ANALYSIS) received FDA 510(k) clearance on 1991-05-21, under 510(k) number K910712.

Who is the listed applicant for VILLAN (VIDEO LIFT LINK ANALYSIS)?

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

What is the FDA product code for VILLAN (VIDEO LIFT LINK ANALYSIS)?

The FDA product code for VILLAN (VIDEO LIFT LINK ANALYSIS) is LXI.

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 Physio Systems, 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.

K871557DISCIPLINE II RTDK870872DISCIPLINE I

Related Devices (Code: LXI)

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.

K930573SYNVASIVE CERAMIC SUTTING BLOCKSynvasive Technology, Inc.K892655ACL DRILL GUIDE SYSTEMBaxter Healthcare CorpK890445PERSONAL ALERT ASSIST DEVICESilent Call Corp.K882407BOW & ARROW DRILL GUIDEInstrument Makar, Inc.K881378PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDEPfizer, Inc.K880739DYONICS DRILL GUIDE/ISOMETER SYSTEMDyonics, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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