Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1)

K-Number: K964977 · 1998-08-31

ApplicantInteractive Living Systems, Inc.
Decision Date1998-08-31
Product CodeLFF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1) is the device name listed in this FDA 510(k) record. The listed applicant is Interactive Living Systems, Inc.. It received FDA 510(k) clearance on 1998-08-31 under 510(k) number K964977. The device is classified under product code LFF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1)?

IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1) is a medical device that received FDA 510(k) clearance on 1998-08-31. The listed applicant is Interactive Living Systems, Inc.. The 510(k) number is K964977.

When did IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1) receive FDA 510(k) clearance?

IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1) received FDA 510(k) clearance on 1998-08-31, under 510(k) number K964977.

Who is the listed applicant for IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1)?

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

What is the FDA product code for IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1)?

The FDA product code for IVOC- INTEGRATED VOICE OPERATED CONTROL UNIT (IVOC-1) is LFF.

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

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.

↑