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FDA 510(k)

CEREC 2 CROWN SOFTWARE

K-Number: K972276 · 1997-08-15

ApplicantSiemens AG
Decision Date1997-08-15
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEREC 2 CROWN SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG. It received FDA 510(k) clearance on 1997-08-15 under 510(k) number K972276. 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 CEREC 2 CROWN SOFTWARE?

CEREC 2 CROWN SOFTWARE is a medical device that received FDA 510(k) clearance on 1997-08-15. The listed applicant is Siemens AG. The 510(k) number is K972276.

When did CEREC 2 CROWN SOFTWARE receive FDA 510(k) clearance?

CEREC 2 CROWN SOFTWARE received FDA 510(k) clearance on 1997-08-15, under 510(k) number K972276.

Who is the listed applicant for CEREC 2 CROWN SOFTWARE?

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

What is the FDA product code for CEREC 2 CROWN SOFTWARE?

The FDA product code for CEREC 2 CROWN SOFTWARE is ELW.

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Other records listing Siemens AG 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.

K123375SYNGO.VIAK110366SYNGO.CT CARDIAC FUNCTIONK071310SYNGO CT ONCOLOGY SOFTWARE PACKAGEK063507SYNGO NEURO PBV CTK063373FLEX LOOP COIL SET 3TK053024SYNGO NEURO DSA CT

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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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