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FDA 510(k)

TERUMO SURGUARD SAFETY SYRINGE

K-Number: K024249 · 2003-02-21

ApplicantTerumo Medical Corp.
Decision Date2003-02-21
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TERUMO SURGUARD SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 2003-02-21 under 510(k) number K024249. 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 TERUMO SURGUARD SAFETY SYRINGE?

TERUMO SURGUARD SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2003-02-21. The listed applicant is Terumo Medical Corp.. The 510(k) number is K024249.

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

TERUMO SURGUARD SAFETY SYRINGE received FDA 510(k) clearance on 2003-02-21, under 510(k) number K024249.

Who is the listed applicant for TERUMO SURGUARD SAFETY SYRINGE?

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

What is the FDA product code for TERUMO SURGUARD SAFETY SYRINGE?

The FDA product code for TERUMO SURGUARD SAFETY SYRINGE is MEG.

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Other records listing Terumo Medical Corp. as applicant

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K111606PINNACLE PRECISION ACCESS SYSTEMK111556GLIDECROSS SUPPORT CATHETERK110540TERUMO SUPPORT CATHETERK102008GLIDESHEATHK091329PINNACLE DESTINATION PERIPHERAL GUIDING SHEATHK082997TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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