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FDA 510(k)

NANOBEAM 940, MODEL 940-900-02

K-Number: K073681 · 2008-12-09

ApplicantDavaray, Inc.
Decision Date2008-12-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NANOBEAM 940, MODEL 940-900-02 is the device name listed in this FDA 510(k) record. The listed applicant is Davaray, Inc.. It received FDA 510(k) clearance on 2008-12-09 under 510(k) number K073681. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NANOBEAM 940, MODEL 940-900-02?

NANOBEAM 940, MODEL 940-900-02 is a medical device that received FDA 510(k) clearance on 2008-12-09. The listed applicant is Davaray, Inc.. The 510(k) number is K073681.

When did NANOBEAM 940, MODEL 940-900-02 receive FDA 510(k) clearance?

NANOBEAM 940, MODEL 940-900-02 received FDA 510(k) clearance on 2008-12-09, under 510(k) number K073681.

Who is the listed applicant for NANOBEAM 940, MODEL 940-900-02?

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

What is the FDA product code for NANOBEAM 940, MODEL 940-900-02?

The FDA product code for NANOBEAM 940, MODEL 940-900-02 is ILY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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