Decision Date1992-04-16
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
BARD URETEROSCOPE DEFLECTION MODULE 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 1992-04-16 under 510(k) number K920750. 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 URETEROSCOPE DEFLECTION MODULE?
BARD URETEROSCOPE DEFLECTION MODULE is a medical device that received FDA 510(k) clearance on 1992-04-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K920750.
When did BARD URETEROSCOPE DEFLECTION MODULE receive FDA 510(k) clearance?
BARD URETEROSCOPE DEFLECTION MODULE received FDA 510(k) clearance on 1992-04-16, under 510(k) number K920750.
Who is the listed applicant for BARD URETEROSCOPE DEFLECTION MODULE?
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 URETEROSCOPE DEFLECTION MODULE?
The FDA product code for BARD URETEROSCOPE DEFLECTION MODULE is FGB.
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Official Source
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