Decision Date1993-07-29
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
BARD SAFE SAMPLING DEVICE 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 1993-07-29 under 510(k) number K925446. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BARD SAFE SAMPLING DEVICE?
BARD SAFE SAMPLING DEVICE is a medical device that received FDA 510(k) clearance on 1993-07-29. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K925446.
When did BARD SAFE SAMPLING DEVICE receive FDA 510(k) clearance?
BARD SAFE SAMPLING DEVICE received FDA 510(k) clearance on 1993-07-29, under 510(k) number K925446.
Who is the listed applicant for BARD SAFE SAMPLING DEVICE?
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 SAFE SAMPLING DEVICE?
The FDA product code for BARD SAFE SAMPLING DEVICE is FMI.
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Official Source
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