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FDA 510(k)

BLOOD TRANSFUSION SET (SANGOFIX)

K-Number: K760381 · 1976-11-02

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

Device Summary

BLOOD TRANSFUSION SET (SANGOFIX) 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 K760381. The device is classified under product code JCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD TRANSFUSION SET (SANGOFIX)?

BLOOD TRANSFUSION SET (SANGOFIX) 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 K760381.

When did BLOOD TRANSFUSION SET (SANGOFIX) receive FDA 510(k) clearance?

BLOOD TRANSFUSION SET (SANGOFIX) received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760381.

Who is the listed applicant for BLOOD TRANSFUSION SET (SANGOFIX)?

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 BLOOD TRANSFUSION SET (SANGOFIX)?

The FDA product code for BLOOD TRANSFUSION SET (SANGOFIX) is JCY.

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 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)K760385EXTENSION SETSK760384STOPPERSK760388CATHETER, VEIN (VENOFIX)

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Related Devices (Code: JCY)

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.

K863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYVas-Cath of Canada , Ltd.K840324SILICONE SUMP DRAIN 20 & 40 FRENCHSuperior Plastic Products Corp.K834615TRIPLE LUMEN INFUSIONCATHETERS-Medical Components, Inc.K831453SILCATH CENTRAL CATHETER TRAY W/18 GAArgon Medical Corp.K831451SILCATH CENTRAL CATHETER TRAY SIZE-Argon Medical Corp.K822096CHEMOTHERAPY INFUSION CATHETERAmerican Heyer Schulte

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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