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FDA 510(k)

NEPTUNE

K-Number: K822947 · 1982-10-26

ApplicantJeneric Ind.
Decision Date1982-10-26
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEPTUNE is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1982-10-26 under 510(k) number K822947. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEPTUNE?

NEPTUNE is a medical device that received FDA 510(k) clearance on 1982-10-26. The listed applicant is Jeneric Ind.. The 510(k) number is K822947.

When did NEPTUNE receive FDA 510(k) clearance?

NEPTUNE received FDA 510(k) clearance on 1982-10-26, under 510(k) number K822947.

Who is the listed applicant for NEPTUNE?

The FDA 510(k) record lists Jeneric Ind. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEPTUNE?

The FDA product code for NEPTUNE is EJH.

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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.

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