FDA 510(k)

PORS-ON

K-Number: K821590 · 1982-06-14

Decision Date1982-06-14

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PORS-ON 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 1982-06-14 under 510(k) number K821590. 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 PORS-ON?

PORS-ON is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is J. Aderer, Inc.. The 510(k) number is K821590.

When did PORS-ON receive FDA 510(k) clearance?

PORS-ON received FDA 510(k) clearance on 1982-06-14, under 510(k) number K821590.

Who is the listed applicant for PORS-ON?

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 PORS-ON?

The FDA product code for PORS-ON 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'K821407DEVA M

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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.