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FDA 510(k)

BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)

K-Number: K895959 · 1989-11-29

ApplicantBrevet, Inc.
Decision Date1989-11-29
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BREVET FLOSS PICK (COLD STERILIZATION FLUIDS) is the device name listed in this FDA 510(k) record. The listed applicant is Brevet, Inc.. It received FDA 510(k) clearance on 1989-11-29 under 510(k) number K895959. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)?

BREVET FLOSS PICK (COLD STERILIZATION FLUIDS) is a medical device that received FDA 510(k) clearance on 1989-11-29. The listed applicant is Brevet, Inc.. The 510(k) number is K895959.

When did BREVET FLOSS PICK (COLD STERILIZATION FLUIDS) receive FDA 510(k) clearance?

BREVET FLOSS PICK (COLD STERILIZATION FLUIDS) received FDA 510(k) clearance on 1989-11-29, under 510(k) number K895959.

Who is the listed applicant for BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)?

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 (COLD STERILIZATION FLUIDS)?

The FDA product code for BREVET FLOSS PICK (COLD STERILIZATION FLUIDS) 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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