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FDA 510(k)

NATURELLE II & LITE II-N72-N74-L

K-Number: K833774 · 1984-01-24

ApplicantJeneric Ind.
Decision Date1984-01-24
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NATURELLE II & LITE II-N72-N74-L is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1984-01-24 under 510(k) number K833774. 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 NATURELLE II & LITE II-N72-N74-L?

NATURELLE II & LITE II-N72-N74-L is a medical device that received FDA 510(k) clearance on 1984-01-24. The listed applicant is Jeneric Ind.. The 510(k) number is K833774.

When did NATURELLE II & LITE II-N72-N74-L receive FDA 510(k) clearance?

NATURELLE II & LITE II-N72-N74-L received FDA 510(k) clearance on 1984-01-24, under 510(k) number K833774.

Who is the listed applicant for NATURELLE II & LITE II-N72-N74-L?

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 NATURELLE II & LITE II-N72-N74-L?

The FDA product code for NATURELLE II & LITE II-N72-N74-L is EJS.

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Related Devices (Code: EJS)

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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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