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FDA 510(k)

EXTAVIPRO STERICAN 30G

K-Number: K131040 · 2013-07-15

ApplicantB.Braun Melsungen AG
Decision Date2013-07-15
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTAVIPRO STERICAN 30G is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Melsungen AG. It received FDA 510(k) clearance on 2013-07-15 under 510(k) number K131040. 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 EXTAVIPRO STERICAN 30G?

EXTAVIPRO STERICAN 30G is a medical device that received FDA 510(k) clearance on 2013-07-15. The listed applicant is B.Braun Melsungen AG. The 510(k) number is K131040.

When did EXTAVIPRO STERICAN 30G receive FDA 510(k) clearance?

EXTAVIPRO STERICAN 30G received FDA 510(k) clearance on 2013-07-15, under 510(k) number K131040.

Who is the listed applicant for EXTAVIPRO STERICAN 30G?

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

What is the FDA product code for EXTAVIPRO STERICAN 30G?

The FDA product code for EXTAVIPRO STERICAN 30G is FMI.

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Related Devices (Code: FMI)

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Official Source

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