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FDA 510(k)

DW 236

K-Number: K905204 · 1991-03-29

ApplicantIvoclar North America, Inc.
Decision Date1991-03-29
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DW 236 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 1991-03-29 under 510(k) number K905204. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DW 236?

DW 236 is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Ivoclar North America, Inc.. The 510(k) number is K905204.

When did DW 236 receive FDA 510(k) clearance?

DW 236 received FDA 510(k) clearance on 1991-03-29, under 510(k) number K905204.

Who is the listed applicant for DW 236?

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 236?

The FDA product code for DW 236 is EJJ.

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

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Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK033434BESTALOYWe Dong Myung Dental Industrial Co., Ltd.K032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb Ardent

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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