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FDA 510(k)

SONY LASER VIDEODISC RECORDING SYSTEM

K-Number: K921275 · 1992-06-10

ApplicantSony Medical Systems
Decision Date1992-06-10
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONY LASER VIDEODISC RECORDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sony Medical Systems. It received FDA 510(k) clearance on 1992-06-10 under 510(k) number K921275. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY LASER VIDEODISC RECORDING SYSTEM?

SONY LASER VIDEODISC RECORDING SYSTEM is a medical device that received FDA 510(k) clearance on 1992-06-10. The listed applicant is Sony Medical Systems. The 510(k) number is K921275.

When did SONY LASER VIDEODISC RECORDING SYSTEM receive FDA 510(k) clearance?

SONY LASER VIDEODISC RECORDING SYSTEM received FDA 510(k) clearance on 1992-06-10, under 510(k) number K921275.

Who is the listed applicant for SONY LASER VIDEODISC RECORDING SYSTEM?

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

What is the FDA product code for SONY LASER VIDEODISC RECORDING SYSTEM?

The FDA product code for SONY LASER VIDEODISC RECORDING SYSTEM is LMB.

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Other records listing Sony Medical 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.

K024188UP-DF500 FILMSTATION DIGITAL FILM IMAGERK970999SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITORK961680SONY DKR-700 DIGITAL STILL RECORDERK931170SONY CARDIAC ANALYSIS AND REVIEW STATION (CARS)K924708CINENET CARDIAC IMAGE NETWORK

Related Devices (Code: LMB)

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.

K992131SAMSUNG RAYPAX LONG TERM ARCHIVESamsung Sds Co., Ltd.K984405ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000Intracom Corp.K983447WISE (II) IMAGE MANAGEMENT SYSTEMSectra-Imtec ABK980243PARAMETER DEVELOPMENTS DICOM ARCHIVAL SERVER, (DAS)/DICOM INTRANET SERVICE (DIS)Parameter Developments, Inc.K973463OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVEO Tech, Inc.K973413ID. STORE (RELEASE 2.0)I.S.G. Technologies, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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