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FDA 510(k)

OPTICAL GUIDANCE PLATFORM

K-Number: K071360 · 2007-06-08

ApplicantVarian Medical Systems, Inc.
Decision Date2007-06-08
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OPTICAL GUIDANCE PLATFORM is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2007-06-08 under 510(k) number K071360. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTICAL GUIDANCE PLATFORM?

OPTICAL GUIDANCE PLATFORM is a medical device that received FDA 510(k) clearance on 2007-06-08. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K071360.

When did OPTICAL GUIDANCE PLATFORM receive FDA 510(k) clearance?

OPTICAL GUIDANCE PLATFORM received FDA 510(k) clearance on 2007-06-08, under 510(k) number K071360.

Who is the listed applicant for OPTICAL GUIDANCE PLATFORM?

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

What is the FDA product code for OPTICAL GUIDANCE PLATFORM?

The FDA product code for OPTICAL GUIDANCE PLATFORM is IYE.

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Other records listing Varian Medical Systems, Inc. as applicant

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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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