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FDA 510(k)

MINIMUS I; MINIMUS III, SANAPHON

K-Number: K942649 · 1994-11-29

ApplicantRud Riester GmbH & CO KG
Decision Date1994-11-29
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIMUS I; MINIMUS III, SANAPHON is the device name listed in this FDA 510(k) record. The listed applicant is Rud Riester GmbH & CO KG. It received FDA 510(k) clearance on 1994-11-29 under 510(k) number K942649. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIMUS I; MINIMUS III, SANAPHON?

MINIMUS I; MINIMUS III, SANAPHON is a medical device that received FDA 510(k) clearance on 1994-11-29. The listed applicant is Rud Riester GmbH & CO KG. The 510(k) number is K942649.

When did MINIMUS I; MINIMUS III, SANAPHON receive FDA 510(k) clearance?

MINIMUS I; MINIMUS III, SANAPHON received FDA 510(k) clearance on 1994-11-29, under 510(k) number K942649.

Who is the listed applicant for MINIMUS I; MINIMUS III, SANAPHON?

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

What is the FDA product code for MINIMUS I; MINIMUS III, SANAPHON?

The FDA product code for MINIMUS I; MINIMUS III, SANAPHON is DXN.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Rud 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.

K944337VARIOUS STETHOSCOPESK942650BIG BENK943461VARIOUS TYPES OF MERCURIALS

Related Devices (Code: DXN)

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.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

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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