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FDA 510(k)

GRESCO N.P. DENTAL ALLOY

K-Number: K854495 · 1985-12-27

ApplicantGresco Products, Inc.
Decision Date1985-12-27
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GRESCO N.P. DENTAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Gresco Products, Inc.. It received FDA 510(k) clearance on 1985-12-27 under 510(k) number K854495. 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 GRESCO N.P. DENTAL ALLOY?

GRESCO N.P. DENTAL ALLOY is a medical device that received FDA 510(k) clearance on 1985-12-27. The listed applicant is Gresco Products, Inc.. The 510(k) number is K854495.

When did GRESCO N.P. DENTAL ALLOY receive FDA 510(k) clearance?

GRESCO N.P. DENTAL ALLOY received FDA 510(k) clearance on 1985-12-27, under 510(k) number K854495.

Who is the listed applicant for GRESCO N.P. DENTAL ALLOY?

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

What is the FDA product code for GRESCO N.P. DENTAL ALLOY?

The FDA product code for GRESCO N.P. DENTAL ALLOY is EJH.

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Other records listing Gresco Products, 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.

K981524PRILANEK913405KAR-D-TEKK910813MET-ETCHK910803ENAMEL ETCHING GELK901973CP-3 DENTAL POLISHING MATERIALK854494CERAM-ETCH

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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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