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FDA 510(k)

RIESS-LUHR

K-Number: K811113 · 1981-06-16

ApplicantAllomedic
Decision Date1981-06-16
Product CodeDZA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RIESS-LUHR is the device name listed in this FDA 510(k) record. The listed applicant is Allomedic. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811113. The device is classified under product code DZA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIESS-LUHR?

RIESS-LUHR is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Allomedic. The 510(k) number is K811113.

When did RIESS-LUHR receive FDA 510(k) clearance?

RIESS-LUHR received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811113.

Who is the listed applicant for RIESS-LUHR?

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

What is the FDA product code for RIESS-LUHR?

The FDA product code for RIESS-LUHR is DZA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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