Decision Date1990-09-27
Product CodeDTP
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
BARD FILTERED CARDIOTOMY RESERVOIR 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 1990-09-27 under 510(k) number K902856. The device is classified under product code DTP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BARD FILTERED CARDIOTOMY RESERVOIR?
BARD FILTERED CARDIOTOMY RESERVOIR is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K902856.
When did BARD FILTERED CARDIOTOMY RESERVOIR receive FDA 510(k) clearance?
BARD FILTERED CARDIOTOMY RESERVOIR received FDA 510(k) clearance on 1990-09-27, under 510(k) number K902856.
Who is the listed applicant for BARD FILTERED CARDIOTOMY RESERVOIR?
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 FILTERED CARDIOTOMY RESERVOIR?
The FDA product code for BARD FILTERED CARDIOTOMY RESERVOIR is DTP.
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Official Source
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