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FDA 510(k)

VIEWPOINT TOOLS- STERRAD

K-Number: K983764 · 1999-07-08

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1999-07-08
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIEWPOINT TOOLS- STERRAD 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 1999-07-08 under 510(k) number K983764. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIEWPOINT TOOLS- STERRAD?

VIEWPOINT TOOLS- STERRAD is a medical device that received FDA 510(k) clearance on 1999-07-08. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K983764.

When did VIEWPOINT TOOLS- STERRAD receive FDA 510(k) clearance?

VIEWPOINT TOOLS- STERRAD received FDA 510(k) clearance on 1999-07-08, under 510(k) number K983764.

Who is the listed applicant for VIEWPOINT TOOLS- STERRAD?

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 VIEWPOINT TOOLS- STERRAD?

The FDA product code for VIEWPOINT TOOLS- STERRAD is HAW.

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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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