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FDA 510(k)

ELECATH INFANT ARTERIAL & VENOUS CANNU

K-Number: K842369 · 1984-08-27

ApplicantElectro-Catheter Corp.
Decision Date1984-08-27
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ELECATH INFANT ARTERIAL & VENOUS CANNU is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Catheter Corp.. It received FDA 510(k) clearance on 1984-08-27 under 510(k) number K842369. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECATH INFANT ARTERIAL & VENOUS CANNU?

ELECATH INFANT ARTERIAL & VENOUS CANNU is a medical device that received FDA 510(k) clearance on 1984-08-27. The listed applicant is Electro-Catheter Corp.. The 510(k) number is K842369.

When did ELECATH INFANT ARTERIAL & VENOUS CANNU receive FDA 510(k) clearance?

ELECATH INFANT ARTERIAL & VENOUS CANNU received FDA 510(k) clearance on 1984-08-27, under 510(k) number K842369.

Who is the listed applicant for ELECATH INFANT ARTERIAL & VENOUS CANNU?

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

What is the FDA product code for ELECATH INFANT ARTERIAL & VENOUS CANNU?

The FDA product code for ELECATH INFANT ARTERIAL & VENOUS CANNU is BWF.

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Other records listing Electro-Catheter Corp. 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.

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Related Devices (Code: BWF)

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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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