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FDA 510(k)

SONY DXC-LS1 COLOR VIDEO CAMERA

K-Number: K980279 · 1998-04-24

ApplicantSony Medical Electronics Co.
Decision Date1998-04-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SONY DXC-LS1 COLOR VIDEO CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Sony Medical Electronics Co.. It received FDA 510(k) clearance on 1998-04-24 under 510(k) number K980279. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY DXC-LS1 COLOR VIDEO CAMERA?

SONY DXC-LS1 COLOR VIDEO CAMERA is a medical device that received FDA 510(k) clearance on 1998-04-24. The listed applicant is Sony Medical Electronics Co.. The 510(k) number is K980279.

When did SONY DXC-LS1 COLOR VIDEO CAMERA receive FDA 510(k) clearance?

SONY DXC-LS1 COLOR VIDEO CAMERA received FDA 510(k) clearance on 1998-04-24, under 510(k) number K980279.

Who is the listed applicant for SONY DXC-LS1 COLOR VIDEO CAMERA?

The FDA 510(k) record lists Sony Medical Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONY DXC-LS1 COLOR VIDEO CAMERA?

The FDA product code for SONY DXC-LS1 COLOR VIDEO CAMERA is GCJ.

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Other records listing Sony Medical Electronics Co. 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.

K913886SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDERK904447SONY CINE VIDEO SYSTEM SME-3500K902535SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEMK901153SONY VO-5800H VIDEOCASSETTE RECORDERK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDK884008SONY CINE VIDEO SYSTEM SME-3300

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Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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.

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