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FDA 510(k)

INTRAVENOUS TRANSFER SET (INTRAFIX)

K-Number: K760380 · 1976-11-02

Decision Date1976-11-02
Product CodeJCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS TRANSFER SET (INTRAFIX) 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 K760380. 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 INTRAVENOUS TRANSFER SET (INTRAFIX)?

INTRAVENOUS TRANSFER SET (INTRAFIX) 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 K760380.

When did INTRAVENOUS TRANSFER SET (INTRAFIX) receive FDA 510(k) clearance?

INTRAVENOUS TRANSFER SET (INTRAFIX) received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760380.

Who is the listed applicant for INTRAVENOUS TRANSFER SET (INTRAFIX)?

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 INTRAVENOUS TRANSFER SET (INTRAFIX)?

The FDA product code for INTRAVENOUS TRANSFER SET (INTRAFIX) 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.

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.

View all 13 devices →

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.

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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