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FDA 510(k)

TELESHARE 910

K-Number: K925793 · 1993-02-26

ApplicantDejarnette Research Systems
Decision Date1993-02-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TELESHARE 910 is the device name listed in this FDA 510(k) record. The listed applicant is Dejarnette Research Systems. It received FDA 510(k) clearance on 1993-02-26 under 510(k) number K925793. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELESHARE 910?

TELESHARE 910 is a medical device that received FDA 510(k) clearance on 1993-02-26. The listed applicant is Dejarnette Research Systems. The 510(k) number is K925793.

When did TELESHARE 910 receive FDA 510(k) clearance?

TELESHARE 910 received FDA 510(k) clearance on 1993-02-26, under 510(k) number K925793.

Who is the listed applicant for TELESHARE 910?

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

What is the FDA product code for TELESHARE 910?

The FDA product code for TELESHARE 910 is LLZ.

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Other records listing Dejarnette Research Systems 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.

K974130VISISHARE IMAGING SYSTEM AND/ OR SOFTWARE, VISISHARE SYSTEM AND/ OR SOFTWAREK973421IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE(2100{SIKARUS X86}/(1500{WINDOWS NT}K973422LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT])K963861LASERSHARE PRINT SPOOLER AND/OR SOFTWAREK963594IMAGESHARE SECONDARY CAPTURE ACQUISITION STATION AND/OR SOFTWARE (1000 FILM DIGITIZER ACQUISITION STATION)K963628IMAGESHARE COMPUTED RADIOGRAPHY ACQUISITION STATION AND/OR SOFTWARE

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Related Devices (Code: LLZ)

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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