TAKE 1 ADVANCE
K-Number: K130869 · 2013-05-30
Advertisement
Device Summary
Frequently Asked Questions
What is the TAKE 1 ADVANCE?
TAKE 1 ADVANCE is a medical device that received FDA 510(k) clearance on 2013-05-30. The listed applicant is Sybron Dental Specialties. The 510(k) number is K130869.
When did TAKE 1 ADVANCE receive FDA 510(k) clearance?
TAKE 1 ADVANCE received FDA 510(k) clearance on 2013-05-30, under 510(k) number K130869.
Who is the listed applicant for TAKE 1 ADVANCE?
The FDA 510(k) record lists Sybron Dental Specialties as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAKE 1 ADVANCE?
The FDA product code for TAKE 1 ADVANCE is ELW.
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 Sybron Dental Specialties 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: ELW)
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