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FDA 510(k)

DW 273 #1

K-Number: K003632 · 2000-12-20

ApplicantIvoclar North America, Inc.
Decision Date2000-12-20
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DW 273 #1 is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar North America, Inc.. It received FDA 510(k) clearance on 2000-12-20 under 510(k) number K003632. 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 DW 273 #1?

DW 273 #1 is a medical device that received FDA 510(k) clearance on 2000-12-20. The listed applicant is Ivoclar North America, Inc.. The 510(k) number is K003632.

When did DW 273 #1 receive FDA 510(k) clearance?

DW 273 #1 received FDA 510(k) clearance on 2000-12-20, under 510(k) number K003632.

Who is the listed applicant for DW 273 #1?

The FDA 510(k) record lists Ivoclar North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DW 273 #1?

The FDA product code for DW 273 #1 is EJS.

Other records listing Ivoclar North America, 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.

K012174ERIS LAYERING MATERIALSK011491HELIOSEAL CLEAR CHROMAK011492IN TEN-SK011490MODIFICATION TO EXCITEK011023D.SIGN 96K011022BIOUNIVERSAL PDF

View all 131 devices →

Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020194SIMIDUR KF PLUSWieland Dental + Technik GmbH & Co. KG

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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