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FDA 510(k)

LASER SYS*STIM 540, MODEL ME 540

K-Number: K043586 · 2005-05-06

ApplicantMettler Electronics Corp.
Decision Date2005-05-06
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LASER SYS*STIM 540, MODEL ME 540 is the device name listed in this FDA 510(k) record. The listed applicant is Mettler Electronics Corp.. It received FDA 510(k) clearance on 2005-05-06 under 510(k) number K043586. 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 LASER SYS*STIM 540, MODEL ME 540?

LASER SYS*STIM 540, MODEL ME 540 is a medical device that received FDA 510(k) clearance on 2005-05-06. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K043586.

When did LASER SYS*STIM 540, MODEL ME 540 receive FDA 510(k) clearance?

LASER SYS*STIM 540, MODEL ME 540 received FDA 510(k) clearance on 2005-05-06, under 510(k) number K043586.

Who is the listed applicant for LASER SYS*STIM 540, MODEL ME 540?

The FDA 510(k) record lists Mettler Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER SYS*STIM 540, MODEL ME 540?

The FDA product code for LASER SYS*STIM 540, MODEL ME 540 is ILY.

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Other records listing Mettler Electronics Corp. 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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