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FDA 510(k)

SYSTEMIC LUPUS

K-Number: K790257 · 1979-03-15

ApplicantIcl Scientific
Decision Date1979-03-15
Product CodeDHC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

SYSTEMIC LUPUS is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1979-03-15 under 510(k) number K790257. The device is classified under product code DHC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSTEMIC LUPUS?

SYSTEMIC LUPUS is a medical device that received FDA 510(k) clearance on 1979-03-15. The listed applicant is Icl Scientific. The 510(k) number is K790257.

When did SYSTEMIC LUPUS receive FDA 510(k) clearance?

SYSTEMIC LUPUS received FDA 510(k) clearance on 1979-03-15, under 510(k) number K790257.

Who is the listed applicant for SYSTEMIC LUPUS?

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

What is the FDA product code for SYSTEMIC LUPUS?

The FDA product code for SYSTEMIC LUPUS is DHC.

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Related Devices (Code: DHC)

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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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