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FDA 510(k)

CONNECTORS

K-Number: K760382 · 1976-11-02

ApplicantB. Braun Instruments
Decision Date1976-11-02
Product CodeGCD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun Instruments. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760382. The device is classified under product code GCD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONNECTORS?

CONNECTORS is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is B. Braun Instruments. The 510(k) number is K760382.

When did CONNECTORS receive FDA 510(k) clearance?

CONNECTORS received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760382.

Who is the listed applicant for CONNECTORS?

The FDA 510(k) record lists B. Braun Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONNECTORS?

The FDA product code for CONNECTORS is GCD.

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Other records listing B. Braun Instruments 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.

K760380INTRAVENOUS TRANSFER SET (INTRAFIX)K760390CATHETER, VEIN (BRAUNULA T)K760385EXTENSION SETSK760384STOPPERSK760388CATHETER, VEIN (VENOFIX)K760381BLOOD TRANSFUSION SET (SANGOFIX)

View all 13 devices →

Related Devices (Code: GCD)

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.

K952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.R-Group Intl.K940198L-CATH CONNECTOR ASSEMBLYLuther Medical Products, Inc.K863446ANGIOMED HIGH PRESSURE CONNECTORSAngiomed U.S., Inc.K851196INCISION DRAINSil-Med Corp.K851921Y CONNECTORSil-Med Corp.K760524CATHETER CONNECTOR, ARGYLE TUBINGSherwood Medical Industries

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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