BLENGOLD SPECIAL
K-Number: K851872 · 1985-07-02
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Device Summary
Frequently Asked Questions
What is the BLENGOLD SPECIAL?
BLENGOLD SPECIAL is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Heraeus Dental Gold Corp.. The 510(k) number is K851872.
When did BLENGOLD SPECIAL receive FDA 510(k) clearance?
BLENGOLD SPECIAL received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851872.
Who is the listed applicant for BLENGOLD SPECIAL?
The FDA 510(k) record lists Heraeus Dental Gold Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLENGOLD SPECIAL?
The FDA product code for BLENGOLD SPECIAL 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 Heraeus Dental Gold Corp. 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.
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