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FDA 510(k)

RELACS 7000

K-Number: K951272 · 1995-05-12

ApplicantMicro-Mega Societe Anonyme
Decision Date1995-05-12
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RELACS 7000 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 1995-05-12 under 510(k) number K951272. 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 RELACS 7000?

RELACS 7000 is a medical device that received FDA 510(k) clearance on 1995-05-12. The listed applicant is Micro-Mega Societe Anonyme. The 510(k) number is K951272.

When did RELACS 7000 receive FDA 510(k) clearance?

RELACS 7000 received FDA 510(k) clearance on 1995-05-12, under 510(k) number K951272.

Who is the listed applicant for RELACS 7000?

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 RELACS 7000?

The FDA product code for RELACS 7000 is ELC.

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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

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Related Devices (Code: ELC)

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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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