Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10

K-Number: K940749 · 1994-03-28

ApplicantAalba Dent, Inc.
Decision Date1994-03-28
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10 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 1994-03-28 under 510(k) number K940749. 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 LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10?

LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10 is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K940749.

When did LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10 receive FDA 510(k) clearance?

LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10 received FDA 510(k) clearance on 1994-03-28, under 510(k) number K940749.

Who is the listed applicant for LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10?

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 LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10?

The FDA product code for LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10 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 VK040179CONTINUMK033356VERASOFT ESK982094VERABOND 2K972971NPG + 2K973265VERABOND 2V

View all 27 devices →

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.

↑