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FDA 510(k)

SONIC AIR MM1500 + (MID), MODEL 50400014

K-Number: K081268 · 2009-08-10

ApplicantMicro-Mega Societe Anonyme
Decision Date2009-08-10
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SONIC AIR MM1500 + (MID), MODEL 50400014 is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Mega Societe Anonyme. It received FDA 510(k) clearance on 2009-08-10 under 510(k) number K081268. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONIC AIR MM1500 + (MID), MODEL 50400014?

SONIC AIR MM1500 + (MID), MODEL 50400014 is a medical device that received FDA 510(k) clearance on 2009-08-10. The listed applicant is Micro-Mega Societe Anonyme. The 510(k) number is K081268.

When did SONIC AIR MM1500 + (MID), MODEL 50400014 receive FDA 510(k) clearance?

SONIC AIR MM1500 + (MID), MODEL 50400014 received FDA 510(k) clearance on 2009-08-10, under 510(k) number K081268.

Who is the listed applicant for SONIC AIR MM1500 + (MID), MODEL 50400014?

The FDA 510(k) record lists Micro-Mega Societe Anonyme as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONIC AIR MM1500 + (MID), MODEL 50400014?

The FDA product code for SONIC AIR MM1500 + (MID), MODEL 50400014 is ELC.

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Other records listing Micro-Mega Societe Anonyme as applicant

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K103123APEX POINTER+; MEASRUING CABLE, HOOK, LIP CLIP, TOUCH PROBE (ACCESSORIES)K042171AX'S ENDO 04, 06, 08, 2.5, 40 , MODELS 50100206, 50100217, 50100218, 50100230, 50100232K971350SERIES XE, SERIES SE, SERIES TEK961275SIRIUS 10, 10L, 40, 40LK961235SIRIUS 180, 180L, 230, 230LK961494SERIES XE 140XE,40XE,10XE/SERIES SE 140SE,40SE,10SE/SERIES 10TE

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Related Devices (Code: ELC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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