Decision Date1996-04-26
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
MM 324 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 1996-04-26 under 510(k) number K961076. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MM 324?
MM 324 is a medical device that received FDA 510(k) clearance on 1996-04-26. The listed applicant is Micro-Mega Societe Anonyme. The 510(k) number is K961076.
When did MM 324 receive FDA 510(k) clearance?
MM 324 received FDA 510(k) clearance on 1996-04-26, under 510(k) number K961076.
Who is the listed applicant for MM 324?
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 MM 324?
The FDA product code for MM 324 is EFB.
Other records listing Micro-Mega Societe Anonyme as applicant
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.
K103123APEX POINTER+; MEASRUING CABLE, HOOK, LIP CLIP, TOUCH PROBE (ACCESSORIES)K081268SONIC AIR MM1500 + (MID), MODEL 50400014K042171AX'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, 230L View all 10 devices →
Related Devices (Code: EFB)
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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.