FDA 510(k)

HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER

K-Number: K061933 · 2006-11-16

Decision Date2006-11-16

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER is the device name listed in this FDA 510(k) record. The listed applicant is Hager Worldwide, Inc.. It received FDA 510(k) clearance on 2006-11-16 under 510(k) number K061933. 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 HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER?

HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER is a medical device that received FDA 510(k) clearance on 2006-11-16. The listed applicant is Hager Worldwide, Inc.. The 510(k) number is K061933.

When did HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER receive FDA 510(k) clearance?

HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER received FDA 510(k) clearance on 2006-11-16, under 510(k) number K061933.

Who is the listed applicant for HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER?

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

What is the FDA product code for HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER?

The FDA product code for HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER is FMI.

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Other records listing Hager Worldwide, Inc. as applicant

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Related Devices (Code: FMI)

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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.