FDA 510(k)

STERICAN HYPODERMIC NEEDLES

K-Number: K072247 · 2007-11-08

Decision Date2007-11-08

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERICAN HYPODERMIC NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2007-11-08 under 510(k) number K072247. 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 STERICAN HYPODERMIC NEEDLES?

STERICAN HYPODERMIC NEEDLES is a medical device that received FDA 510(k) clearance on 2007-11-08. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K072247.

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

STERICAN HYPODERMIC NEEDLES received FDA 510(k) clearance on 2007-11-08, under 510(k) number K072247.

Who is the listed applicant for STERICAN HYPODERMIC NEEDLES?

The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERICAN HYPODERMIC NEEDLES?

The FDA product code for STERICAN HYPODERMIC NEEDLES is FMI.

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Related Devices (Code: FMI)

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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.