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FDA 510(k)

STECO-TITANMAGNETICS

K-Number: K990979 · 1999-09-03

ApplicantSteco-System-Technik GmbH & Cokg
Decision Date1999-09-03
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STECO-TITANMAGNETICS is the device name listed in this FDA 510(k) record. The listed applicant is Steco-System-Technik GmbH & Cokg. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K990979. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STECO-TITANMAGNETICS?

STECO-TITANMAGNETICS is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Steco-System-Technik GmbH & Cokg. The 510(k) number is K990979.

When did STECO-TITANMAGNETICS receive FDA 510(k) clearance?

STECO-TITANMAGNETICS received FDA 510(k) clearance on 1999-09-03, under 510(k) number K990979.

Who is the listed applicant for STECO-TITANMAGNETICS?

The FDA 510(k) record lists Steco-System-Technik GmbH & Cokg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STECO-TITANMAGNETICS?

The FDA product code for STECO-TITANMAGNETICS is EGG.

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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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