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FDA 510(k)

SONY DKR-700 DIGITAL STILL RECORDER

K-Number: K961680 · 1996-07-03

ApplicantSony Medical Systems
Decision Date1996-07-03
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONY DKR-700 DIGITAL STILL RECORDER 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 1996-07-03 under 510(k) number K961680. 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 DKR-700 DIGITAL STILL RECORDER?

SONY DKR-700 DIGITAL STILL RECORDER is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Sony Medical Systems. The 510(k) number is K961680.

When did SONY DKR-700 DIGITAL STILL RECORDER receive FDA 510(k) clearance?

SONY DKR-700 DIGITAL STILL RECORDER received FDA 510(k) clearance on 1996-07-03, under 510(k) number K961680.

Who is the listed applicant for SONY DKR-700 DIGITAL STILL RECORDER?

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 DKR-700 DIGITAL STILL RECORDER?

The FDA product code for SONY DKR-700 DIGITAL STILL RECORDER 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 MONITORK931170SONY CARDIAC ANALYSIS AND REVIEW STATION (CARS)K924708CINENET CARDIAC IMAGE NETWORKK921275SONY LASER VIDEODISC RECORDING SYSTEM

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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