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)

VISTA 4000 SIGMA

K-Number: K925600 · 1993-02-08

ApplicantUnitron Industries, Inc.
Decision Date1993-02-08
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VISTA 4000 SIGMA is the device name listed in this FDA 510(k) record. The listed applicant is Unitron Industries, Inc.. It received FDA 510(k) clearance on 1993-02-08 under 510(k) number K925600. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA 4000 SIGMA?

VISTA 4000 SIGMA is a medical device that received FDA 510(k) clearance on 1993-02-08. The listed applicant is Unitron Industries, Inc.. The 510(k) number is K925600.

When did VISTA 4000 SIGMA receive FDA 510(k) clearance?

VISTA 4000 SIGMA received FDA 510(k) clearance on 1993-02-08, under 510(k) number K925600.

Who is the listed applicant for VISTA 4000 SIGMA?

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

What is the FDA product code for VISTA 4000 SIGMA?

The FDA product code for VISTA 4000 SIGMA is ESD.

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 Unitron Industries, 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.

K974339UNITRON MODEL SOUND F/XD PROGRAMMABLEK974340UNITRON MODEL SOUND F/XP PROGRAMMABLE MINI BTEK974338UNITRON MODEL F/X PROGRAMMABLE (MINI BTE)K970692UNITRON MODEL SOUND F/X CICK970519UNITRON MODEL SOUND F/X PROGRAMMABLE ITE (SF/X PROGRAMMABLE)K964508UNITRON MODEL ICON AOHP +4 (ICON AOHP +4)

View all 69 devices →

Related Devices (Code: ESD)

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.

K232999Lyric4 Hearing AidSonova AGK130790LYRIC2Phonak, LLCK081136LYRIC HEARING AIDInsound Medical, Inc.K021867INSOUND XT SERIES HEARING AIDInsound Medical, Inc.K003558TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)Siemens Hearing Instruments, Inc.K984518SONIC INNOVATIONS COMPLETELY-IN-THE-CANAL DSP HEARING AID WITH SOFT SHELLSonic Innovations, Inc.

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.

↑