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FDA 510(k)

NATURDOM

K-Number: K790433 · 1979-10-04

ApplicantJuan C. Lucena
Decision Date1979-10-04
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NATURDOM is the device name listed in this FDA 510(k) record. The listed applicant is Juan C. Lucena. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K790433. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATURDOM?

NATURDOM is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Juan C. Lucena. The 510(k) number is K790433.

When did NATURDOM receive FDA 510(k) clearance?

NATURDOM received FDA 510(k) clearance on 1979-10-04, under 510(k) number K790433.

Who is the listed applicant for NATURDOM?

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

What is the FDA product code for NATURDOM?

The FDA product code for NATURDOM is HIS.

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Related Devices (Code: HIS)

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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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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