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FDA 510(k)

OVUS CAPLESS SAFETY NEEDLE

K-Number: K013006 · 2002-02-06

ApplicantOvus Systems
Decision Date2002-02-06
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OVUS CAPLESS SAFETY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ovus Systems. It received FDA 510(k) clearance on 2002-02-06 under 510(k) number K013006. 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 OVUS CAPLESS SAFETY NEEDLE?

OVUS CAPLESS SAFETY NEEDLE is a medical device that received FDA 510(k) clearance on 2002-02-06. The listed applicant is Ovus Systems. The 510(k) number is K013006.

When did OVUS CAPLESS SAFETY NEEDLE receive FDA 510(k) clearance?

OVUS CAPLESS SAFETY NEEDLE received FDA 510(k) clearance on 2002-02-06, under 510(k) number K013006.

Who is the listed applicant for OVUS CAPLESS SAFETY NEEDLE?

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

What is the FDA product code for OVUS CAPLESS SAFETY NEEDLE?

The FDA product code for OVUS CAPLESS SAFETY NEEDLE 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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