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FDA 510(k)

SPECIAL WHITE

K-Number: K820318 · 1982-03-02

ApplicantJ. Aderer, Inc.
Decision Date1982-03-02
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPECIAL WHITE 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 1982-03-02 under 510(k) number K820318. 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 SPECIAL WHITE?

SPECIAL WHITE is a medical device that received FDA 510(k) clearance on 1982-03-02. The listed applicant is J. Aderer, Inc.. The 510(k) number is K820318.

When did SPECIAL WHITE receive FDA 510(k) clearance?

SPECIAL WHITE received FDA 510(k) clearance on 1982-03-02, under 510(k) number K820318.

Who is the listed applicant for SPECIAL WHITE?

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 SPECIAL WHITE?

The FDA product code for SPECIAL WHITE is EJT.

Related Clinical Trials

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.

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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 CASTK822957PURCASTK82179882 ALLOYK821832DEGUCAST UK821572DUALLOR 'R'K821590PORS-ON

View all 24 devices →

Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-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

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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