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FDA 510(k)

STEMPRO MSC SFM

K-Number: K103302 · 2011-02-18

ApplicantLife Technologies Corporation
Decision Date2011-02-18
Product CodeNDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STEMPRO MSC SFM is the device name listed in this FDA 510(k) record. The listed applicant is Life Technologies Corporation. It received FDA 510(k) clearance on 2011-02-18 under 510(k) number K103302. The device is classified under product code NDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEMPRO MSC SFM?

STEMPRO MSC SFM is a medical device that received FDA 510(k) clearance on 2011-02-18. The listed applicant is Life Technologies Corporation. The 510(k) number is K103302.

When did STEMPRO MSC SFM receive FDA 510(k) clearance?

STEMPRO MSC SFM received FDA 510(k) clearance on 2011-02-18, under 510(k) number K103302.

Who is the listed applicant for STEMPRO MSC SFM?

The FDA 510(k) record lists Life Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEMPRO MSC SFM?

The FDA product code for STEMPRO MSC SFM is NDS.

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Related Devices (Code: NDS)

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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.

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