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FDA 510(k)

SOLOGUARD LOCKING PLUS SYRINGE

K-Number: K993609 · 2000-03-17

ApplicantSafeguard Medical Products, Inc.
Decision Date2000-03-17
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLOGUARD LOCKING PLUS SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Safeguard Medical Products, Inc.. It received FDA 510(k) clearance on 2000-03-17 under 510(k) number K993609. 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 SOLOGUARD LOCKING PLUS SYRINGE?

SOLOGUARD LOCKING PLUS SYRINGE is a medical device that received FDA 510(k) clearance on 2000-03-17. The listed applicant is Safeguard Medical Products, Inc.. The 510(k) number is K993609.

When did SOLOGUARD LOCKING PLUS SYRINGE receive FDA 510(k) clearance?

SOLOGUARD LOCKING PLUS SYRINGE received FDA 510(k) clearance on 2000-03-17, under 510(k) number K993609.

Who is the listed applicant for SOLOGUARD LOCKING PLUS SYRINGE?

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

What is the FDA product code for SOLOGUARD LOCKING PLUS SYRINGE?

The FDA product code for SOLOGUARD LOCKING PLUS 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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