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FDA 510(k)

CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA

K-Number: K851913 · 1985-09-16

ApplicantCordis Corp.
Decision Date1985-09-16
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1985-09-16 under 510(k) number K851913. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA?

CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Cordis Corp.. The 510(k) number is K851913.

When did CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA receive FDA 510(k) clearance?

CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA received FDA 510(k) clearance on 1985-09-16, under 510(k) number K851913.

Who is the listed applicant for CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA?

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

What is the FDA product code for CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA?

The FDA product code for CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA is LDF.

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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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