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FDA 510(k)

NEEDLE-TRAP/NEEDLE SAFETY LABEL

K-Number: K073206 · 2008-01-16

ApplicantSchreiner Medipharm
Decision Date2008-01-16
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLE-TRAP/NEEDLE SAFETY LABEL is the device name listed in this FDA 510(k) record. The listed applicant is Schreiner Medipharm. It received FDA 510(k) clearance on 2008-01-16 under 510(k) number K073206. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE-TRAP/NEEDLE SAFETY LABEL?

NEEDLE-TRAP/NEEDLE SAFETY LABEL is a medical device that received FDA 510(k) clearance on 2008-01-16. The listed applicant is Schreiner Medipharm. The 510(k) number is K073206.

When did NEEDLE-TRAP/NEEDLE SAFETY LABEL receive FDA 510(k) clearance?

NEEDLE-TRAP/NEEDLE SAFETY LABEL received FDA 510(k) clearance on 2008-01-16, under 510(k) number K073206.

Who is the listed applicant for NEEDLE-TRAP/NEEDLE SAFETY LABEL?

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

What is the FDA product code for NEEDLE-TRAP/NEEDLE SAFETY LABEL?

The FDA product code for NEEDLE-TRAP/NEEDLE SAFETY LABEL is MEG.

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Related Devices (Code: MEG)

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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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