FG DIAMOND BURRS
K-Number: K900089 · 1990-04-03
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Device Summary
Frequently Asked Questions
What is the FG DIAMOND BURRS?
FG DIAMOND BURRS is a medical device that received FDA 510(k) clearance on 1990-04-03. The listed applicant is Kab Gloves Unltd.. The 510(k) number is K900089.
When did FG DIAMOND BURRS receive FDA 510(k) clearance?
FG DIAMOND BURRS received FDA 510(k) clearance on 1990-04-03, under 510(k) number K900089.
Who is the listed applicant for FG DIAMOND BURRS?
The FDA 510(k) record lists Kab Gloves Unltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FG DIAMOND BURRS?
The FDA product code for FG DIAMOND BURRS is DZP.
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 Kab Gloves Unltd. 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: DZP)
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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