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FDA 510(k)

MICRO 2 SYSTEM

K-Number: K900785 · 1990-04-16

ApplicantInodent
Decision Date1990-04-16
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO 2 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Inodent. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K900785. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO 2 SYSTEM?

MICRO 2 SYSTEM is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Inodent. The 510(k) number is K900785.

When did MICRO 2 SYSTEM receive FDA 510(k) clearance?

MICRO 2 SYSTEM received FDA 510(k) clearance on 1990-04-16, under 510(k) number K900785.

Who is the listed applicant for MICRO 2 SYSTEM?

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

What is the FDA product code for MICRO 2 SYSTEM?

The FDA product code for MICRO 2 SYSTEM is EGG.

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Related Devices (Code: EGG)

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.

K990979STECO-TITANMAGNETICSSteco-System-Technik GmbH & CokgK950259COUPLING DEVICE FOR DENTAL PROSTHESISDr. Joseph E. Grasso, D.D.S.K925700ZEST ANCHOR ADVANCED GENERATIONZest Anchors, Inc.K915299COGAN CORP KITS OF DENTAL HAND INSTRUMENTSCogan Corp.K912435DENTAL CONNECTOR PRECISION ATTACHMENTMetalor Dental USA Corp.K912567CONICAST, INTRACAST, OMECASTMetalor Dental USA Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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