Decision Date1999-03-09
Product CodeDTP
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR 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 1999-03-09 under 510(k) number K990514. 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 MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR?
MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR is a medical device that received FDA 510(k) clearance on 1999-03-09. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K990514.
When did MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR receive FDA 510(k) clearance?
MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR received FDA 510(k) clearance on 1999-03-09, under 510(k) number K990514.
Who is the listed applicant for MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR?
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 MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR?
The FDA product code for MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR is DTP.
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Official Source
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