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FDA 510(k)

LIFEJET PRINTER 400

K-Number: K011617 · 2001-06-08

ApplicantFerrania S.P.A. Stabilimento DI Ferrania
Decision Date2001-06-08
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIFEJET PRINTER 400 is the device name listed in this FDA 510(k) record. The listed applicant is Ferrania S.P.A. Stabilimento DI Ferrania. It received FDA 510(k) clearance on 2001-06-08 under 510(k) number K011617. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEJET PRINTER 400?

LIFEJET PRINTER 400 is a medical device that received FDA 510(k) clearance on 2001-06-08. The listed applicant is Ferrania S.P.A. Stabilimento DI Ferrania. The 510(k) number is K011617.

When did LIFEJET PRINTER 400 receive FDA 510(k) clearance?

LIFEJET PRINTER 400 received FDA 510(k) clearance on 2001-06-08, under 510(k) number K011617.

Who is the listed applicant for LIFEJET PRINTER 400?

The FDA 510(k) record lists Ferrania S.P.A. Stabilimento DI Ferrania as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFEJET PRINTER 400?

The FDA product code for LIFEJET PRINTER 400 is LMC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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