Decision Date1990-05-17
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
BARD SHORT RIGID URETEROSCOPE 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 1990-05-17 under 510(k) number K900813. The device is classified under product code FGB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BARD SHORT RIGID URETEROSCOPE?
BARD SHORT RIGID URETEROSCOPE is a medical device that received FDA 510(k) clearance on 1990-05-17. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K900813.
When did BARD SHORT RIGID URETEROSCOPE receive FDA 510(k) clearance?
BARD SHORT RIGID URETEROSCOPE received FDA 510(k) clearance on 1990-05-17, under 510(k) number K900813.
Who is the listed applicant for BARD SHORT RIGID URETEROSCOPE?
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 SHORT RIGID URETEROSCOPE?
The FDA product code for BARD SHORT RIGID URETEROSCOPE is FGB.
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Official Source
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