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FDA 510(k)

CLINIX MP

K-Number: K960920 · 1996-05-20

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1996-05-20
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLINIX MP is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1996-05-20 under 510(k) number K960920. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINIX MP?

CLINIX MP is a medical device that received FDA 510(k) clearance on 1996-05-20. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K960920.

When did CLINIX MP receive FDA 510(k) clearance?

CLINIX MP received FDA 510(k) clearance on 1996-05-20, under 510(k) number K960920.

Who is the listed applicant for CLINIX MP?

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

What is the FDA product code for CLINIX MP?

The FDA product code for CLINIX MP is OWB.

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Related Devices (Code: OWB)

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.

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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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