PALLIAG NF III
K-Number: K883036 · 1988-08-12
Advertisement
Device Summary
Frequently Asked Questions
What is the PALLIAG NF III?
PALLIAG NF III is a medical device that received FDA 510(k) clearance on 1988-08-12. The listed applicant is Degussa Dental, Inc.. The 510(k) number is K883036.
When did PALLIAG NF III receive FDA 510(k) clearance?
PALLIAG NF III received FDA 510(k) clearance on 1988-08-12, under 510(k) number K883036.
Who is the listed applicant for PALLIAG NF III?
The FDA 510(k) record lists Degussa Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PALLIAG NF III?
The FDA product code for PALLIAG NF III 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 Degussa Dental, 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.
Advertisement