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FDA 510(k)

MS NONPRECIOUS CROWN & BRIDGE ALLOY

K-Number: K842377 · 1984-07-31

ApplicantDental Ventures of America, Inc.
Decision Date1984-07-31
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MS NONPRECIOUS CROWN & BRIDGE ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Dental Ventures of America, Inc.. It received FDA 510(k) clearance on 1984-07-31 under 510(k) number K842377. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS NONPRECIOUS CROWN & BRIDGE ALLOY?

MS NONPRECIOUS CROWN & BRIDGE ALLOY is a medical device that received FDA 510(k) clearance on 1984-07-31. The listed applicant is Dental Ventures of America, Inc.. The 510(k) number is K842377.

When did MS NONPRECIOUS CROWN & BRIDGE ALLOY receive FDA 510(k) clearance?

MS NONPRECIOUS CROWN & BRIDGE ALLOY received FDA 510(k) clearance on 1984-07-31, under 510(k) number K842377.

Who is the listed applicant for MS NONPRECIOUS CROWN & BRIDGE ALLOY?

The FDA 510(k) record lists Dental Ventures of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MS NONPRECIOUS CROWN & BRIDGE ALLOY?

The FDA product code for MS NONPRECIOUS CROWN & BRIDGE ALLOY is EJH.

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Other records listing Dental Ventures of America, Inc. 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.

K000894C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MOK780808PIEZOMATIC ULTRASONIC SCALER (SYSTEM S)

Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K032136WIROBOND CBego U.S.A.

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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