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FDA 510(k)

PHILIPS ANGIOPRO

K-Number: K911888 · 1991-10-15

ApplicantPhilips Medical Systems North America, Inc.
Decision Date1991-10-15
Product CodeIZP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS ANGIOPRO is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America, Inc.. It received FDA 510(k) clearance on 1991-10-15 under 510(k) number K911888. The device is classified under product code IZP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS ANGIOPRO?

PHILIPS ANGIOPRO is a medical device that received FDA 510(k) clearance on 1991-10-15. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K911888.

When did PHILIPS ANGIOPRO receive FDA 510(k) clearance?

PHILIPS ANGIOPRO received FDA 510(k) clearance on 1991-10-15, under 510(k) number K911888.

Who is the listed applicant for PHILIPS ANGIOPRO?

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

What is the FDA product code for PHILIPS ANGIOPRO?

The FDA product code for PHILIPS ANGIOPRO is IZP.

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Other records listing Philips Medical Systems North America, 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.

K102005ALLURA XPER OR TABLE SERIESK062233HEARTSTART MRX MONITOR/DEFIBRILLATORK062283THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORSK061052THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90K050151MULTIDIAGNOST ELEVAK042867PHILIPS ORTHOPAEDIC APPLICATIONS

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Related Devices (Code: IZP)

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.

K934944MPQ-42Elema-Schonander, Inc.K904144PULMOVISION CHEST RADIOGRAPHY X-RAY SYSTEMMallinckrodt Group, Inc.K904103SEP 90Elema-Schonander, Inc.K874451OMNIPLANE 200 FILM CHANGER SYSTEMMedrad, Inc.K854251THE CSE FILM CHANGER SYSTEMChanger Service & Engineering, Inc.K842903SEP PROGRAMMER FOR PUCK U & UD FILMCHANGElema-Schonander, 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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