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FDA 510(k)

STERN'S S250 NORDAM

K-Number: K092917 · 2010-06-24

ApplicantCefla S.C.
Decision Date2010-06-24
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STERN'S S250 NORDAM is the device name listed in this FDA 510(k) record. The listed applicant is Cefla S.C.. It received FDA 510(k) clearance on 2010-06-24 under 510(k) number K092917. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERN'S S250 NORDAM?

STERN'S S250 NORDAM is a medical device that received FDA 510(k) clearance on 2010-06-24. The listed applicant is Cefla S.C.. The 510(k) number is K092917.

When did STERN'S S250 NORDAM receive FDA 510(k) clearance?

STERN'S S250 NORDAM received FDA 510(k) clearance on 2010-06-24, under 510(k) number K092917.

Who is the listed applicant for STERN'S S250 NORDAM?

The FDA 510(k) record lists Cefla S.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERN'S S250 NORDAM?

The FDA product code for STERN'S S250 NORDAM is EIA.

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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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