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FDA 510(k)

CONVERSIL FL AND CONVERSIL P

K-Number: K913583 · 1991-11-13

ApplicantWilde-USA, Inc.
Decision Date1991-11-13
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONVERSIL FL AND CONVERSIL P 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 1991-11-13 under 510(k) number K913583. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERSIL FL AND CONVERSIL P?

CONVERSIL FL AND CONVERSIL P is a medical device that received FDA 510(k) clearance on 1991-11-13. The listed applicant is Wilde-USA, Inc.. The 510(k) number is K913583.

When did CONVERSIL FL AND CONVERSIL P receive FDA 510(k) clearance?

CONVERSIL FL AND CONVERSIL P received FDA 510(k) clearance on 1991-11-13, under 510(k) number K913583.

Who is the listed applicant for CONVERSIL FL AND CONVERSIL P?

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 CONVERSIL FL AND CONVERSIL P?

The FDA product code for CONVERSIL FL AND CONVERSIL P is ELW.

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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: ELW)

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.

K254152Dia-X Sil Light BodyDiaDent Group InternationalK254142Dia-X Sil Heavy BodyDiaDent Group InternationalK254112Dia-X Sil BiteDiaDent Group InternationalK253501Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium Regular Set - 454g (1lb) (052327); Chroma Print Premium Fast Set - 454g (1lb) (052457); Chroma Print Premium Regular Set - 454g (1lb) (051460); Perfil Pro - 454g (1lb) (056213); Perfil Pro+ - 454g (1lb) (056121); Perfil Pro Chroma - 454g (1lb) (056122); Hydro Print Premium Fast Set - Multi Pack (056205); Hydro Print Premium Regular Set - Multi Pack (056208); Hydro Print Premium Fast Set - 9,07Kg (20lb) (056204);Vigodent Indústria E Comercio LtdaK250969JET BITE; JET BLUE BITE FAST; JET BLUE BITE SUPERFASTDent4you AGK241924Elastic Impression MaterialBeijing Okvd Biological Technology , Ltd.

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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