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FDA 510(k)

LUPO-TEC

K-Number: K782129 · 1979-03-12

ApplicantArmkel, LLC
Decision Date1979-03-12
Product CodeDHC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LUPO-TEC is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 1979-03-12 under 510(k) number K782129. 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 LUPO-TEC?

LUPO-TEC is a medical device that received FDA 510(k) clearance on 1979-03-12. The listed applicant is Armkel, LLC. The 510(k) number is K782129.

When did LUPO-TEC receive FDA 510(k) clearance?

LUPO-TEC received FDA 510(k) clearance on 1979-03-12, under 510(k) number K782129.

Who is the listed applicant for LUPO-TEC?

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

What is the FDA product code for LUPO-TEC?

The FDA product code for LUPO-TEC is 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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