FORGET - DENTURE BONDING LIQUID
K-Number: K791576 · 1979-10-26
Advertisement
Device Summary
Frequently Asked Questions
What is the FORGET - DENTURE BONDING LIQUID?
FORGET - DENTURE BONDING LIQUID is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Norcliff Thayer, Inc.. The 510(k) number is K791576.
When did FORGET - DENTURE BONDING LIQUID receive FDA 510(k) clearance?
FORGET - DENTURE BONDING LIQUID received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791576.
Who is the listed applicant for FORGET - DENTURE BONDING LIQUID?
The FDA 510(k) record lists Norcliff Thayer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORGET - DENTURE BONDING LIQUID?
The FDA product code for FORGET - DENTURE BONDING LIQUID is KOL.
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 Norcliff Thayer, 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: KOL)
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