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FDA 510(k)

MAGNEFORCE

K-Number: K943068 · 1994-08-17

ApplicantOrmco Corp.
Decision Date1994-08-17
Product CodeECO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAGNEFORCE is the device name listed in this FDA 510(k) record. The listed applicant is Ormco Corp.. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K943068. The device is classified under product code ECO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNEFORCE?

MAGNEFORCE is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Ormco Corp.. The 510(k) number is K943068.

When did MAGNEFORCE receive FDA 510(k) clearance?

MAGNEFORCE received FDA 510(k) clearance on 1994-08-17, under 510(k) number K943068.

Who is the listed applicant for MAGNEFORCE?

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

What is the FDA product code for MAGNEFORCE?

The FDA product code for MAGNEFORCE is ECO.

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Related Devices (Code: ECO)

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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