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FDA 510(k)

WEBERNEEDLE BASIC LASER

K-Number: K073352 · 2008-08-11

ApplicantWeber Medical GmbH
Decision Date2008-08-11
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WEBERNEEDLE BASIC LASER is the device name listed in this FDA 510(k) record. The listed applicant is Weber Medical GmbH. It received FDA 510(k) clearance on 2008-08-11 under 510(k) number K073352. 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 WEBERNEEDLE BASIC LASER?

WEBERNEEDLE BASIC LASER is a medical device that received FDA 510(k) clearance on 2008-08-11. The listed applicant is Weber Medical GmbH. The 510(k) number is K073352.

When did WEBERNEEDLE BASIC LASER receive FDA 510(k) clearance?

WEBERNEEDLE BASIC LASER received FDA 510(k) clearance on 2008-08-11, under 510(k) number K073352.

Who is the listed applicant for WEBERNEEDLE BASIC LASER?

The FDA 510(k) record lists Weber Medical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEBERNEEDLE BASIC LASER?

The FDA product code for WEBERNEEDLE BASIC LASER 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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