Decision Date1988-09-06
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER 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 1988-09-06 under 510(k) number K882330. 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 BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER?
BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER is a medical device that received FDA 510(k) clearance on 1988-09-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K882330.
When did BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER receive FDA 510(k) clearance?
BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER received FDA 510(k) clearance on 1988-09-06, under 510(k) number K882330.
Who is the listed applicant for BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER?
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 BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER?
The FDA product code for BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER 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.