BREVET FLOSS PICK (AUTOCLAVE STERILIZER)
K-Number: K895958 · 1989-12-04
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Device Summary
Frequently Asked Questions
What is the BREVET FLOSS PICK (AUTOCLAVE STERILIZER)?
BREVET FLOSS PICK (AUTOCLAVE STERILIZER) is a medical device that received FDA 510(k) clearance on 1989-12-04. The listed applicant is Brevet, Inc.. The 510(k) number is K895958.
When did BREVET FLOSS PICK (AUTOCLAVE STERILIZER) receive FDA 510(k) clearance?
BREVET FLOSS PICK (AUTOCLAVE STERILIZER) received FDA 510(k) clearance on 1989-12-04, under 510(k) number K895958.
Who is the listed applicant for BREVET FLOSS PICK (AUTOCLAVE STERILIZER)?
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 BREVET FLOSS PICK (AUTOCLAVE STERILIZER)?
The FDA product code for BREVET FLOSS PICK (AUTOCLAVE STERILIZER) is EKJ.
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: EKJ)
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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