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FDA 510(k)

SCICAN CLASSIC

K-Number: K984556 · 1999-02-09

ApplicantScholly Fiberoptic GmbH
Decision Date1999-02-09
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SCICAN CLASSIC is the device name listed in this FDA 510(k) record. The listed applicant is Scholly Fiberoptic GmbH. It received FDA 510(k) clearance on 1999-02-09 under 510(k) number K984556. 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 SCICAN CLASSIC?

SCICAN CLASSIC is a medical device that received FDA 510(k) clearance on 1999-02-09. The listed applicant is Scholly Fiberoptic GmbH. The 510(k) number is K984556.

When did SCICAN CLASSIC receive FDA 510(k) clearance?

SCICAN CLASSIC received FDA 510(k) clearance on 1999-02-09, under 510(k) number K984556.

Who is the listed applicant for SCICAN CLASSIC?

The FDA 510(k) record lists Scholly Fiberoptic GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCICAN CLASSIC?

The FDA product code for SCICAN CLASSIC is EIA.

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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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