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FDA 510(k)

RITRACT SAFETY SYRINGE

K-Number: K060002 · 2006-06-02

ApplicantRitract , Ltd.
Decision Date2006-06-02
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RITRACT SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Ritract , Ltd.. It received FDA 510(k) clearance on 2006-06-02 under 510(k) number K060002. 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 RITRACT SAFETY SYRINGE?

RITRACT SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2006-06-02. The listed applicant is Ritract , Ltd.. The 510(k) number is K060002.

When did RITRACT SAFETY SYRINGE receive FDA 510(k) clearance?

RITRACT SAFETY SYRINGE received FDA 510(k) clearance on 2006-06-02, under 510(k) number K060002.

Who is the listed applicant for RITRACT SAFETY SYRINGE?

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

What is the FDA product code for RITRACT SAFETY SYRINGE?

The FDA product code for RITRACT SAFETY SYRINGE is 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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