FDA 510(k)

BEGOPAL 300

K-Number: K983081 · 1998-10-28

ApplicantBego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

Decision Date1998-10-28

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

BEGOPAL 300 is the device name listed in this FDA 510(k) record. The listed applicant is Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. It received FDA 510(k) clearance on 1998-10-28 under 510(k) number K983081. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEGOPAL 300?

BEGOPAL 300 is a medical device that received FDA 510(k) clearance on 1998-10-28. The listed applicant is Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. The 510(k) number is K983081.

When did BEGOPAL 300 receive FDA 510(k) clearance?

BEGOPAL 300 received FDA 510(k) clearance on 1998-10-28, under 510(k) number K983081.

Who is the listed applicant for BEGOPAL 300?

The FDA 510(k) record lists Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEGOPAL 300?

The FDA product code for BEGOPAL 300 is EJS.

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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.