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FDA 510(k)

BREVET DISPOSABLE CONNECTORS

K-Number: K895753 · 1989-11-14

ApplicantBrevet, Inc.
Decision Date1989-11-14
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BREVET DISPOSABLE CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Brevet, Inc.. It received FDA 510(k) clearance on 1989-11-14 under 510(k) number K895753. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BREVET DISPOSABLE CONNECTORS?

BREVET DISPOSABLE CONNECTORS is a medical device that received FDA 510(k) clearance on 1989-11-14. The listed applicant is Brevet, Inc.. The 510(k) number is K895753.

When did BREVET DISPOSABLE CONNECTORS receive FDA 510(k) clearance?

BREVET DISPOSABLE CONNECTORS received FDA 510(k) clearance on 1989-11-14, under 510(k) number K895753.

Who is the listed applicant for BREVET DISPOSABLE CONNECTORS?

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 DISPOSABLE CONNECTORS?

The FDA product code for BREVET DISPOSABLE CONNECTORS is DQY.

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.

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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.

K910794SMALL INSTRUMENT STERILIZATION/BUR BOXK895958BREVET FLOSS PICK (AUTOCLAVE STERILIZER)K895959BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)K883126BREVET DENTAL INSTRUMENTSK882617BREVET CASSETTE STERILIZATION MODULE

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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