FDA 510(k)

NPG + 2

K-Number: K972971 · 1998-01-05

Decision Date1998-01-05

Product CodeEJH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

NPG + 2 is the device name listed in this FDA 510(k) record. The listed applicant is Aalba Dent, Inc.. It received FDA 510(k) clearance on 1998-01-05 under 510(k) number K972971. 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 NPG + 2?

NPG + 2 is a medical device that received FDA 510(k) clearance on 1998-01-05. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K972971.

When did NPG + 2 receive FDA 510(k) clearance?

NPG + 2 received FDA 510(k) clearance on 1998-01-05, under 510(k) number K972971.

Who is the listed applicant for NPG + 2?

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

What is the FDA product code for NPG + 2?

The FDA product code for NPG + 2 is EJH.

Other records listing Aalba Dent, 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.

K040180CONTINUM V K040179CONTINUM K033356VERASOFT ES K982094VERABOND 2 K973265VERABOND 2V K972607PLATALLOY

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Related Devices (Code: EJH)

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO K040180CONTINUM 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

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