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FDA 510(k)

SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM

K-Number: K902535 · 1990-06-29

ApplicantSony Medical Electronics Co.
Decision Date1990-06-29
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM 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 1990-06-29 under 510(k) number K902535. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM?

SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM is a medical device that received FDA 510(k) clearance on 1990-06-29. The listed applicant is Sony Medical Electronics Co.. The 510(k) number is K902535.

When did SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM receive FDA 510(k) clearance?

SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM received FDA 510(k) clearance on 1990-06-29, under 510(k) number K902535.

Who is the listed applicant for SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM?

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 WBS-700H VIDEOCASSETTE RECORDER SYSTEM?

The FDA product code for SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEM is JAA.

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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.

K980279SONY DXC-LS1 COLOR VIDEO CAMERAK913886SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDERK904447SONY CINE VIDEO SYSTEM SME-3500K901153SONY VO-5800H VIDEOCASSETTE RECORDERK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDK884008SONY CINE VIDEO SYSTEM SME-3300

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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