QUEST 2 AND 20
K-Number: K945910 · 1994-12-29
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Device Summary
Frequently Asked Questions
What is the QUEST 2 AND 20?
QUEST 2 AND 20 is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K945910.
When did QUEST 2 AND 20 receive FDA 510(k) clearance?
QUEST 2 AND 20 received FDA 510(k) clearance on 1994-12-29, under 510(k) number K945910.
Who is the listed applicant for QUEST 2 AND 20?
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 QUEST 2 AND 20?
The FDA product code for QUEST 2 AND 20 is EJT.
Related Clinical Trials
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.
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.
Related Devices (Code: EJT)
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.
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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