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FDA 510(k)

E.N.S.I. SYRINGE

K-Number: K000572 · 2000-02-24

ApplicantTri-Ject Intl. Corp.
Decision Date2000-02-24
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

E.N.S.I. SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Ject Intl. Corp.. It received FDA 510(k) clearance on 2000-02-24 under 510(k) number K000572. 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 E.N.S.I. SYRINGE?

E.N.S.I. SYRINGE is a medical device that received FDA 510(k) clearance on 2000-02-24. The listed applicant is Tri-Ject Intl. Corp.. The 510(k) number is K000572.

When did E.N.S.I. SYRINGE receive FDA 510(k) clearance?

E.N.S.I. SYRINGE received FDA 510(k) clearance on 2000-02-24, under 510(k) number K000572.

Who is the listed applicant for E.N.S.I. SYRINGE?

The FDA 510(k) record lists Tri-Ject Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E.N.S.I. SYRINGE?

The FDA product code for E.N.S.I. 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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