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FDA 510(k)

NUTROMAT

K-Number: K831325 · 1983-06-02

ApplicantMedlog GmbH Marketing Services
Decision Date1983-06-02
Product CodeGBB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NUTROMAT is the device name listed in this FDA 510(k) record. The listed applicant is Medlog GmbH Marketing Services. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K831325. The device is classified under product code GBB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUTROMAT?

NUTROMAT is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Medlog GmbH Marketing Services. The 510(k) number is K831325.

When did NUTROMAT receive FDA 510(k) clearance?

NUTROMAT received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831325.

Who is the listed applicant for NUTROMAT?

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

What is the FDA product code for NUTROMAT?

The FDA product code for NUTROMAT is GBB.

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 Medlog GmbH Marketing Services 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.

K832086USE 77 ULTRASONIC NEBULIZERK830913MINITROP AEROSAL, PRODOMO AEROSAL ANDK813455PUMP & DETECTORK810155DOP 84

Related Devices (Code: GBB)

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.

K964102TENET TIBIAL FRACTURE SUPPORTTenet Medical EngineeringK893598HYDRAULIC FOOT OPERATED STOOLArthro-Medic, Inc.K831385LITHOTOMY CHAIR #415Midmark Corp.K822264NAGASHIMA SN OPERATOR'S CHAIRKelleher Corp.K822251EXAMINATION & TREATMENT CHAIRSKelleher Corp.K822013NAGASHIMA SN AUTOMATIC TREATMENT CHAIRKelleher Corp.

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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