FDA 510(k)

CANNULA CADDY

K-Number: K781866 · 1978-11-15

Decision Date1978-11-15

Product Code

DecisionSubstantially Equivalent

Device Summary

CANNULA CADDY is the device name listed in this FDA 510(k) record. The listed applicant is Katena Products, Inc.. It received FDA 510(k) clearance on 1978-11-15 under 510(k) number K781866. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA CADDY?

CANNULA CADDY is a medical device that received FDA 510(k) clearance on 1978-11-15. The listed applicant is Katena Products, Inc.. The 510(k) number is K781866.

When did CANNULA CADDY receive FDA 510(k) clearance?

CANNULA CADDY received FDA 510(k) clearance on 1978-11-15, under 510(k) number K781866.

Who is the listed applicant for CANNULA CADDY?

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

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Other records listing Katena Products, Inc. as applicant

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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.