ALGINATE/SILICONE CROWN & BRIDGE MATER
K-Number: K802990 · 1981-02-02
Advertisement
Device Summary
Frequently Asked Questions
What is the ALGINATE/SILICONE CROWN & BRIDGE MATER?
ALGINATE/SILICONE CROWN & BRIDGE MATER is a medical device that received FDA 510(k) clearance on 1981-02-02. The listed applicant is Buffalo Dental Mfg. Co., Inc.. The 510(k) number is K802990.
When did ALGINATE/SILICONE CROWN & BRIDGE MATER receive FDA 510(k) clearance?
ALGINATE/SILICONE CROWN & BRIDGE MATER received FDA 510(k) clearance on 1981-02-02, under 510(k) number K802990.
Who is the listed applicant for ALGINATE/SILICONE CROWN & BRIDGE MATER?
The FDA 510(k) record lists Buffalo Dental Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALGINATE/SILICONE CROWN & BRIDGE MATER?
The FDA product code for ALGINATE/SILICONE CROWN & BRIDGE MATER 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 Buffalo Dental Mfg. Co., 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: 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