FDA 510(k)

DW232 #31

K-Number: K932774 · 1993-10-20

Decision Date1993-10-20

Product CodeEJT

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DW232 #31 is the device name listed in this FDA 510(k) record. The listed applicant is Invoclar North America, Inc.. It received FDA 510(k) clearance on 1993-10-20 under 510(k) number K932774. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DW232 #31?

DW232 #31 is a medical device that received FDA 510(k) clearance on 1993-10-20. The listed applicant is Invoclar North America, Inc.. The 510(k) number is K932774.

When did DW232 #31 receive FDA 510(k) clearance?

DW232 #31 received FDA 510(k) clearance on 1993-10-20, under 510(k) number K932774.

Who is the listed applicant for DW232 #31?

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

What is the FDA product code for DW232 #31?

The FDA product code for DW232 #31 is EJT.

Other records listing Invoclar 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.

K920560DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL

Related Devices (Code: EJT)

K052463PROMETAL HN86Prometal Technologies K041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KG K040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KG K040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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.