FDA 510(k)

DEVA 4

K-Number: K832530 · 1983-09-29

Decision Date1983-09-29

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DEVA 4 is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Dental, Inc.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832530. 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 DEVA 4?

DEVA 4 is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Degussa Dental, Inc.. The 510(k) number is K832530.

When did DEVA 4 receive FDA 510(k) clearance?

DEVA 4 received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832530.

Who is the listed applicant for DEVA 4?

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

What is the FDA product code for DEVA 4?

The FDA product code for DEVA 4 is EJS.

Other records listing Degussa Dental, 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.

K883758ALBABOND 60 K883511ALBABOND E K883508HERA H K883509HERAEUS DG 63 K883510DEGUPAL 4 K883507HERAEUS C SPECIAL

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Related Devices (Code: EJS)

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KG K022252STERNGOLD 1, MODEL 1127781Sterngold K022469ECO E4Wieland Dental + Technik GmbH & Co. KG K021367STERNGOLD 66, MODEL #1180230Sterngold K020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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.