Small Volume Syringe

FDA 510(k) K062865 · Alcon Laboratories

Substantially Equivalent

510(k) numberK062865

Submission

Device name
Small Volume Syringe
Applicant
Alcon Laboratories
Fort Worth, TX, US
Received
September 25, 2006
Decision date
August 23, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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Questions and answers

When was Small Volume Syringe cleared by the FDA?

Small Volume Syringe (K062865) received a 510(k) decision of Substantially Equivalent on August 23, 2007, 332 days after the submission was received.

What is the product code of K062865?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.