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FDA 510(k)

ECLIPSE

K-Number: K030981 · 2003-06-24

ApplicantVarian Medical Systems, Inc.
Decision Date2003-06-24
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECLIPSE 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 2003-06-24 under 510(k) number K030981. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECLIPSE?

ECLIPSE is a medical device that received FDA 510(k) clearance on 2003-06-24. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K030981.

When did ECLIPSE receive FDA 510(k) clearance?

ECLIPSE received FDA 510(k) clearance on 2003-06-24, under 510(k) number K030981.

Who is the listed applicant for ECLIPSE?

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 ECLIPSE?

The FDA product code for ECLIPSE is LNH.

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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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