FDA 510(k)

MICRO 2 HYPODERMIC NEEDLES

K-Number: K830242 · 1983-02-15

Decision Date1983-02-15

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MICRO 2 HYPODERMIC NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Mpl Division. It received FDA 510(k) clearance on 1983-02-15 under 510(k) number K830242. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO 2 HYPODERMIC NEEDLES?

MICRO 2 HYPODERMIC NEEDLES is a medical device that received FDA 510(k) clearance on 1983-02-15. The listed applicant is Smith & Nephew, Mpl Division. The 510(k) number is K830242.

When did MICRO 2 HYPODERMIC NEEDLES receive FDA 510(k) clearance?

MICRO 2 HYPODERMIC NEEDLES received FDA 510(k) clearance on 1983-02-15, under 510(k) number K830242.

Who is the listed applicant for MICRO 2 HYPODERMIC NEEDLES?

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

What is the FDA product code for MICRO 2 HYPODERMIC NEEDLES?

The FDA product code for MICRO 2 HYPODERMIC NEEDLES is FMI.

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Other records listing Smith & Nephew, Mpl Division as applicant

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Related Devices (Code: FMI)

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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.