SCALEX 800
K-Number: K954820 · 1996-01-18
Advertisement
Device Summary
Frequently Asked Questions
What is the SCALEX 800?
SCALEX 800 is a medical device that received FDA 510(k) clearance on 1996-01-18. The listed applicant is Dentamerica. The 510(k) number is K954820.
When did SCALEX 800 receive FDA 510(k) clearance?
SCALEX 800 received FDA 510(k) clearance on 1996-01-18, under 510(k) number K954820.
Who is the listed applicant for SCALEX 800?
The FDA 510(k) record lists Dentamerica as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCALEX 800?
The FDA product code for SCALEX 800 is ELC.
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 Dentamerica 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: ELC)
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.
Advertisement