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FDA 510(k)

CONVERBASE

K-Number: K912990 · 1992-03-25

ApplicantWilde-USA, Inc.
Decision Date1992-03-25
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONVERBASE is the device name listed in this FDA 510(k) record. The listed applicant is Wilde-USA, Inc.. It received FDA 510(k) clearance on 1992-03-25 under 510(k) number K912990. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERBASE?

CONVERBASE is a medical device that received FDA 510(k) clearance on 1992-03-25. The listed applicant is Wilde-USA, Inc.. The 510(k) number is K912990.

When did CONVERBASE receive FDA 510(k) clearance?

CONVERBASE received FDA 510(k) clearance on 1992-03-25, under 510(k) number K912990.

Who is the listed applicant for CONVERBASE?

The FDA 510(k) record lists Wilde-USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVERBASE?

The FDA product code for CONVERBASE is EBI.

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Other records listing Wilde-USA, Inc. 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.

K913582COMPATIT RK915653KERAMAILK913581WILDE ADHESIVE BONDING SYSTEMK923472COMPACOLORK920649COMPASEPK915250WIL-PDS & WIL-PDI CASTING ALLOYS

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Related Devices (Code: EBI)

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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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