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FDA 510(k)

ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6

K-Number: K051922 · 2005-09-14

ApplicantCynosure, Inc.
Decision Date2005-09-14
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6 is the device name listed in this FDA 510(k) record. The listed applicant is Cynosure, Inc.. It received FDA 510(k) clearance on 2005-09-14 under 510(k) number K051922. 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 ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6?

ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6 is a medical device that received FDA 510(k) clearance on 2005-09-14. The listed applicant is Cynosure, Inc.. The 510(k) number is K051922.

When did ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6 receive FDA 510(k) clearance?

ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6 received FDA 510(k) clearance on 2005-09-14, under 510(k) number K051922.

Who is the listed applicant for ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6?

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

What is the FDA product code for ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6?

The FDA product code for ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6 is ILY.

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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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