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FDA 510(k)

NPG 2 BASE METAL ALLOY

K-Number: K892419 · 1989-06-16

ApplicantAalba Dent, Inc.
Decision Date1989-06-16
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NPG 2 BASE METAL ALLOY 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 1989-06-16 under 510(k) number K892419. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NPG 2 BASE METAL ALLOY?

NPG 2 BASE METAL ALLOY is a medical device that received FDA 510(k) clearance on 1989-06-16. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K892419.

When did NPG 2 BASE METAL ALLOY receive FDA 510(k) clearance?

NPG 2 BASE METAL ALLOY received FDA 510(k) clearance on 1989-06-16, under 510(k) number K892419.

Who is the listed applicant for NPG 2 BASE METAL ALLOY?

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 BASE METAL ALLOY?

The FDA product code for NPG 2 BASE METAL ALLOY is EJF.

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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 VK040179CONTINUMK033356VERASOFT ESK982094VERABOND 2K972971NPG + 2K973265VERABOND 2V

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Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, Inc.

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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