FDA 510(k)

SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS

K-Number: K980092 · 1998-03-09

Decision Date1998-03-09

Product CodeFRN

Advisory CommitteeHO

DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1998-03-09 under 510(k) number K980092. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS?

SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS is a medical device that received FDA 510(k) clearance on 1998-03-09. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K980092.

When did SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS receive FDA 510(k) clearance?

SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS received FDA 510(k) clearance on 1998-03-09, under 510(k) number K980092.

Who is the listed applicant for SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS?

The FDA product code for SMITH & NEPHEW DYONICS INTELIJET REUSABLE CANNULAS is FRN.

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Official Source

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