DIAMONDS BURS-COMPOSIT FINISHING
K-Number: K854690 · 1986-03-25
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Device Summary
Frequently Asked Questions
What is the DIAMONDS BURS-COMPOSIT FINISHING?
DIAMONDS BURS-COMPOSIT FINISHING is a medical device that received FDA 510(k) clearance on 1986-03-25. The listed applicant is Almore Intl., Inc.. The 510(k) number is K854690.
When did DIAMONDS BURS-COMPOSIT FINISHING receive FDA 510(k) clearance?
DIAMONDS BURS-COMPOSIT FINISHING received FDA 510(k) clearance on 1986-03-25, under 510(k) number K854690.
Who is the listed applicant for DIAMONDS BURS-COMPOSIT FINISHING?
The FDA 510(k) record lists Almore Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAMONDS BURS-COMPOSIT FINISHING?
The FDA product code for DIAMONDS BURS-COMPOSIT FINISHING is EJL.
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 Almore Intl., 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: EJL)
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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