Decision Date1995-07-10
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
CAPCARD is the device name listed in this FDA 510(k) record. The listed applicant is Capcard, Inc.. It received FDA 510(k) clearance on 1995-07-10 under 510(k) number K942930. 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 CAPCARD?
CAPCARD is a medical device that received FDA 510(k) clearance on 1995-07-10. The listed applicant is Capcard, Inc.. The 510(k) number is K942930.
When did CAPCARD receive FDA 510(k) clearance?
CAPCARD received FDA 510(k) clearance on 1995-07-10, under 510(k) number K942930.
Who is the listed applicant for CAPCARD?
The FDA 510(k) record lists Capcard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAPCARD?
The FDA product code for CAPCARD is FMI.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.