FDA 510(k)

STERICAN CANNULA

K-Number: K131842 · 2013-08-20

Decision Date2013-08-20

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERICAN CANNULA 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 2013-08-20 under 510(k) number K131842. 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 CANNULA?

STERICAN CANNULA is a medical device that received FDA 510(k) clearance on 2013-08-20. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K131842.

When did STERICAN CANNULA receive FDA 510(k) clearance?

STERICAN CANNULA received FDA 510(k) clearance on 2013-08-20, under 510(k) number K131842.

Who is the listed applicant for STERICAN CANNULA?

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 CANNULA?

The FDA product code for STERICAN CANNULA is 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.