FDA 510(k)

DEVA M

K-Number: K821407 · 1982-06-09

Decision Date1982-06-09

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DEVA M is the device name listed in this FDA 510(k) record. The listed applicant is J. Aderer, Inc.. It received FDA 510(k) clearance on 1982-06-09 under 510(k) number K821407. 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 M?

DEVA M is a medical device that received FDA 510(k) clearance on 1982-06-09. The listed applicant is J. Aderer, Inc.. The 510(k) number is K821407.

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

DEVA M received FDA 510(k) clearance on 1982-06-09, under 510(k) number K821407.

Who is the listed applicant for DEVA M?

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

What is the FDA product code for DEVA M?

The FDA product code for DEVA M is EJS.

Other records listing J. Aderer, 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.

K822956G CAST K822957PURCAST K82179882 ALLOY K821832DEGUCAST U K821572DUALLOR 'R'K821590PORS-ON

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.