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FDA 510(k)

EXTENSION SETS

K-Number: K760385 · 1976-11-02

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

Device Summary

EXTENSION SETS 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 K760385. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSION SETS?

EXTENSION SETS 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 K760385.

When did EXTENSION SETS receive FDA 510(k) clearance?

EXTENSION SETS received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760385.

Who is the listed applicant for EXTENSION SETS?

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 EXTENSION SETS?

The FDA product code for EXTENSION SETS is KGZ.

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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)K760382CONNECTORSK760390CATHETER, VEIN (BRAUNULA T)K760384STOPPERSK760388CATHETER, VEIN (VENOFIX)K760381BLOOD TRANSFUSION SET (SANGOFIX)

View all 13 devices →

Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

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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