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FDA 510(k)

INZOMA NP

K-Number: K813418 · 1982-01-07

ApplicantJ. Aderer, Inc.
Decision Date1982-01-07
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INZOMA NP 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 1982-01-07 under 510(k) number K813418. 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 INZOMA NP?

INZOMA NP is a medical device that received FDA 510(k) clearance on 1982-01-07. The listed applicant is J. Aderer, Inc.. The 510(k) number is K813418.

When did INZOMA NP receive FDA 510(k) clearance?

INZOMA NP received FDA 510(k) clearance on 1982-01-07, under 510(k) number K813418.

Who is the listed applicant for INZOMA NP?

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 INZOMA NP?

The FDA product code for INZOMA NP is EJS.

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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: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR 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.

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