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FDA 510(k)

NOMAD (BASE UNIT/PORTABLE UNIT)

K-Number: K872449 · 1987-07-21

ApplicantMinnesota Valley Engineering, Inc.
Decision Date1987-07-21
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NOMAD (BASE UNIT/PORTABLE UNIT) is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Valley Engineering, Inc.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872449. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOMAD (BASE UNIT/PORTABLE UNIT)?

NOMAD (BASE UNIT/PORTABLE UNIT) is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Minnesota Valley Engineering, Inc.. The 510(k) number is K872449.

When did NOMAD (BASE UNIT/PORTABLE UNIT) receive FDA 510(k) clearance?

NOMAD (BASE UNIT/PORTABLE UNIT) received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872449.

Who is the listed applicant for NOMAD (BASE UNIT/PORTABLE UNIT)?

The FDA 510(k) record lists Minnesota Valley Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOMAD (BASE UNIT/PORTABLE UNIT)?

The FDA product code for NOMAD (BASE UNIT/PORTABLE UNIT) is BYJ.

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 Minnesota Valley Engineering, Inc. 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.

K882328HI FLOW 50K875352HI FLOW PORTABLE LIQUID OXYGEN UNITK880101LIBERATOR 53/STROLLER 50

Related Devices (Code: BYJ)

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.

K130068DISMOUNTED MEDICAL & SUPPLEMENTAL OXYGEN SYSTEM (DMOS)Essex Industries, Inc. D/B/A Essex Cryogenics of MK113767MOUNTED MEDICAL OXYGEN SYSTEMEssex Industries, Inc.K103324PRECISION LIQUID OXYGEN SYSTEMPrecision Medical, Inc.K101272MASS OXYGEN DISTRIBUTION SYSTEM (MODS) MODEL 10C-0061-3Essex Industries, Inc.K081779GOLOX-93Respironics, Inc.K080023MODIFICATION TO: SPIRITCaire, 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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