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FDA 510(k)

CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.)

K-Number: K946041 · 1995-06-16

ApplicantCardico, Inc.
Decision Date1995-06-16
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.) is the device name listed in this FDA 510(k) record. The listed applicant is Cardico, Inc.. It received FDA 510(k) clearance on 1995-06-16 under 510(k) number K946041. 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 CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.)?

CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.) is a medical device that received FDA 510(k) clearance on 1995-06-16. The listed applicant is Cardico, Inc.. The 510(k) number is K946041.

When did CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.) receive FDA 510(k) clearance?

CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.) received FDA 510(k) clearance on 1995-06-16, under 510(k) number K946041.

Who is the listed applicant for CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.)?

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

What is the FDA product code for CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.)?

The FDA product code for CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.) is FMI.

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Official Source

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