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FDA 510(k)

RI-MINI

K-Number: K932503 · 1993-10-08

ApplicantRudolf Riester GmbH & Co. KG
Decision Date1993-10-08
Product CodeERA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RI-MINI is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Riester GmbH & Co. KG. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K932503. The device is classified under product code ERA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RI-MINI?

RI-MINI is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Rudolf Riester GmbH & Co. KG. The 510(k) number is K932503.

When did RI-MINI receive FDA 510(k) clearance?

RI-MINI received FDA 510(k) clearance on 1993-10-08, under 510(k) number K932503.

Who is the listed applicant for RI-MINI?

The FDA 510(k) record lists Rudolf Riester GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RI-MINI?

The FDA product code for RI-MINI is ERA.

Other records listing Rudolf Riester GmbH & Co. KG as applicant

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.

K002954RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERSK002955EMPIRE N BLOOD PRESSURE MANOMETERSK972377RI-MEGAK972378SANAPHON NK972379PRECISA NK972301BIG BEN SQUARE, BIG BEN ROUND

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Related Devices (Code: ERA)

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.

K123821AIO HD OTOSCOPEBlue FocusK121326LANTOS 3D EAR SCANNERLantos TechnologiesK110326OSRAM ITOSOsram Sylvania, Inc.K945264OPTUS OTOSCOPESOptus, Inc.K955043WELCH ALLYN BI-OTOSCOPEWelch Allyn, Inc.K952578WELCH ALLY OTOSCOPEWelch Allyn, Inc.

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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