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FDA 510(k)

RF CHOKE CABLE

K-Number: K771750 · 1977-09-30

ApplicantC.R. Bard, Inc.
Decision Date1977-09-30
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RF CHOKE CABLE is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1977-09-30 under 510(k) number K771750. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RF CHOKE CABLE?

RF CHOKE CABLE is a medical device that received FDA 510(k) clearance on 1977-09-30. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K771750.

When did RF CHOKE CABLE receive FDA 510(k) clearance?

RF CHOKE CABLE received FDA 510(k) clearance on 1977-09-30, under 510(k) number K771750.

Who is the listed applicant for RF CHOKE CABLE?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RF CHOKE CABLE?

The FDA product code for RF CHOKE CABLE is DSA.

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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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