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FDA 510(k)

CAPCADDY

K-Number: K880621 · 1988-04-18

ApplicantCapcad, Inc.
Decision Date1988-04-18
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAPCADDY is the device name listed in this FDA 510(k) record. The listed applicant is Capcad, Inc.. It received FDA 510(k) clearance on 1988-04-18 under 510(k) number K880621. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPCADDY?

CAPCADDY is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Capcad, Inc.. The 510(k) number is K880621.

When did CAPCADDY receive FDA 510(k) clearance?

CAPCADDY received FDA 510(k) clearance on 1988-04-18, under 510(k) number K880621.

Who is the listed applicant for CAPCADDY?

The FDA 510(k) record lists Capcad, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAPCADDY?

The FDA product code for CAPCADDY is EJI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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