SMALL INSTRUMENT STERILIZATION/BUR BOX
K-Number: K910794 · 1991-05-23
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Device Summary
Frequently Asked Questions
What is the SMALL INSTRUMENT STERILIZATION/BUR BOX?
SMALL INSTRUMENT STERILIZATION/BUR BOX is a medical device that received FDA 510(k) clearance on 1991-05-23. The listed applicant is Brevet, Inc.. The 510(k) number is K910794.
When did SMALL INSTRUMENT STERILIZATION/BUR BOX receive FDA 510(k) clearance?
SMALL INSTRUMENT STERILIZATION/BUR BOX received FDA 510(k) clearance on 1991-05-23, under 510(k) number K910794.
Who is the listed applicant for SMALL INSTRUMENT STERILIZATION/BUR BOX?
The FDA 510(k) record lists Brevet, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SMALL INSTRUMENT STERILIZATION/BUR BOX?
The FDA product code for SMALL INSTRUMENT STERILIZATION/BUR BOX 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 Brevet, 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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