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FDA 510(k)

PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION

K-Number: K810183 · 1981-02-25

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1981-02-25
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION 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 1981-02-25 under 510(k) number K810183. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION?

PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K810183.

When did PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION receive FDA 510(k) clearance?

PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810183.

Who is the listed applicant for PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION?

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 PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION?

The FDA product code for PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION is IZI.

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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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