Decision Date1985-09-16
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD 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 1985-09-16 under 510(k) number K852513. 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 115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD?
115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K852513.
When did 115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD receive FDA 510(k) clearance?
115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD received FDA 510(k) clearance on 1985-09-16, under 510(k) number K852513.
Who is the listed applicant for 115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD?
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 115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD?
The FDA product code for 115-GK BARD CARE TRANSLU VENTRICULAR PACING LEAD 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.