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FDA 510(k)

HOWMEDICA BRASS CENTER DISC

K-Number: K790640 · 1979-05-01

ApplicantE.C. Moore Co.
Decision Date1979-05-01
Product CodeEHJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HOWMEDICA BRASS CENTER DISC is the device name listed in this FDA 510(k) record. The listed applicant is E.C. Moore Co.. It received FDA 510(k) clearance on 1979-05-01 under 510(k) number K790640. The device is classified under product code EHJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOWMEDICA BRASS CENTER DISC?

HOWMEDICA BRASS CENTER DISC is a medical device that received FDA 510(k) clearance on 1979-05-01. The listed applicant is E.C. Moore Co.. The 510(k) number is K790640.

When did HOWMEDICA BRASS CENTER DISC receive FDA 510(k) clearance?

HOWMEDICA BRASS CENTER DISC received FDA 510(k) clearance on 1979-05-01, under 510(k) number K790640.

Who is the listed applicant for HOWMEDICA BRASS CENTER DISC?

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

What is the FDA product code for HOWMEDICA BRASS CENTER DISC?

The FDA product code for HOWMEDICA BRASS CENTER DISC is EHJ.

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Related Devices (Code: EHJ)

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.

K911111MICROMILLS, PATRIOTS, ALPHA GOLD DIAMONDSVermont Diamond InstrumentsK873002MIN-IDENTOFLEXCentrix, Inc.K771658IDENTOFLEXCavitron 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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