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FDA 510(k)

PROV-KB

K-Number: K960938 · 1996-04-18

ApplicantSilicon-Und Composite Spezialitaten GmbH
Decision Date1996-04-18
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROV-KB is the device name listed in this FDA 510(k) record. The listed applicant is Silicon-Und Composite Spezialitaten GmbH. It received FDA 510(k) clearance on 1996-04-18 under 510(k) number K960938. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROV-KB?

PROV-KB is a medical device that received FDA 510(k) clearance on 1996-04-18. The listed applicant is Silicon-Und Composite Spezialitaten GmbH. The 510(k) number is K960938.

When did PROV-KB receive FDA 510(k) clearance?

PROV-KB received FDA 510(k) clearance on 1996-04-18, under 510(k) number K960938.

Who is the listed applicant for PROV-KB?

The FDA 510(k) record lists Silicon-Und Composite Spezialitaten GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROV-KB?

The FDA product code for PROV-KB is EBG.

Other records listing Silicon-Und Composite Spezialitaten GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K992001TRAY-LINKK991450ETCHING GELK953476MULTI-PRIME AKA/MONO-PRIME

Related Devices (Code: EBG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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