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FDA 510(k)

CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I

K-Number: K854562 · 1986-01-09

ApplicantMedelec Intl. Corp.
Decision Date1986-01-09
Product CodeBRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I is the device name listed in this FDA 510(k) record. The listed applicant is Medelec Intl. Corp.. It received FDA 510(k) clearance on 1986-01-09 under 510(k) number K854562. The device is classified under product code BRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I?

CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I is a medical device that received FDA 510(k) clearance on 1986-01-09. The listed applicant is Medelec Intl. Corp.. The 510(k) number is K854562.

When did CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I receive FDA 510(k) clearance?

CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I received FDA 510(k) clearance on 1986-01-09, under 510(k) number K854562.

Who is the listed applicant for CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I?

The FDA 510(k) record lists Medelec Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I?

The FDA product code for CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I is BRZ.

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Related Devices (Code: BRZ)

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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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