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FDA 510(k)

PHILIPS DSI SYSTEM RELEASE 3.2

K-Number: K920793 · 1992-07-17

ApplicantPhilips Medical Systems, Inc.
Decision Date1992-07-17
Product CodeIZJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS DSI SYSTEM RELEASE 3.2 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1992-07-17 under 510(k) number K920793. The device is classified under product code IZJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS DSI SYSTEM RELEASE 3.2?

PHILIPS DSI SYSTEM RELEASE 3.2 is a medical device that received FDA 510(k) clearance on 1992-07-17. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K920793.

When did PHILIPS DSI SYSTEM RELEASE 3.2 receive FDA 510(k) clearance?

PHILIPS DSI SYSTEM RELEASE 3.2 received FDA 510(k) clearance on 1992-07-17, under 510(k) number K920793.

Who is the listed applicant for PHILIPS DSI SYSTEM RELEASE 3.2?

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

What is the FDA product code for PHILIPS DSI SYSTEM RELEASE 3.2?

The FDA product code for PHILIPS DSI SYSTEM RELEASE 3.2 is IZJ.

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Other records listing Philips Medical Systems, Inc. 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.

K093355PCR ELEVA 1.2K090808PINNACLE3 SMARTARCK071391PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521K063783PHILIPS REUSABLE SPO2 SENSORS M1191T, M1192T AND M1193T, CLIP SENSOR M1196T AND DISPOSABLE SPO2 SENSORS M1131A, M1132AK041741M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE F.0 AND M4840A PHILIPS TELEMETRY SYSTEM II INCLUDING M4841A PATIENK040955M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE E.01 AND INTELLIVUE CLINICAL NETWORK ON VLAN

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Related Devices (Code: IZJ)

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.

K024085CCD CAMERA, MODEL PKP-06000-000Perkins Electronics Co.K972130DISPOSABLE CAMERA COVER, ENCLOSED: DISPOSABLE CAMERA COVER, PERFORATED: DISPOSABLE MICROSCOPE COVER (VARIOUS):X-RAY COVRFairmontmedicalK945580DSP OPTIONPhilips Medical Systems (Cleveland), Inc.K896615CINE CAMERA CONTROL MODEL PK2037Perkins Mfg. Co.K881688DTV-4114 FLUOROSCOPIC TELEVISION CAMERAAdac LaboratoriesK853983CANON X-RAY 35MM CINE CAMERA CSI-35Canon USA, 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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