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FDA 510(k)

SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR

K-Number: K970999 · 1997-05-20

ApplicantSony Medical Systems
Decision Date1997-05-20
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR 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 1997-05-20 under 510(k) number K970999. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR?

SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR is a medical device that received FDA 510(k) clearance on 1997-05-20. The listed applicant is Sony Medical Systems. The 510(k) number is K970999.

When did SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR receive FDA 510(k) clearance?

SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR received FDA 510(k) clearance on 1997-05-20, under 510(k) number K970999.

Who is the listed applicant for SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR?

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 PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR?

The FDA product code for SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR is JAK.

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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 IMAGERK961680SONY DKR-700 DIGITAL STILL RECORDERK931170SONY CARDIAC ANALYSIS AND REVIEW STATION (CARS)K924708CINENET CARDIAC IMAGE NETWORKK921275SONY LASER VIDEODISC RECORDING SYSTEM

Related Devices (Code: JAK)

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.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, LLC

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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