Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PRECISION BLENDER

K-Number: K053232 · 2006-01-10

ApplicantPrecision Medical, Inc.
Decision Date2006-01-10
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRECISION BLENDER is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 2006-01-10 under 510(k) number K053232. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION BLENDER?

PRECISION BLENDER is a medical device that received FDA 510(k) clearance on 2006-01-10. The listed applicant is Precision Medical, Inc.. The 510(k) number is K053232.

When did PRECISION BLENDER receive FDA 510(k) clearance?

PRECISION BLENDER received FDA 510(k) clearance on 2006-01-10, under 510(k) number K053232.

Who is the listed applicant for PRECISION BLENDER?

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

What is the FDA product code for PRECISION BLENDER?

The FDA product code for PRECISION BLENDER is BZR.

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 Precision Medical, 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.

K173807Accu O2 Oxygen AnalyzerK103563PRECISION PORTABLE OXYGEN CONCENTRATION MODEL 4150K103324PRECISION LIQUID OXYGEN SYSTEMK090781HELIO2 BLENDERK072348PRECISION OXYGEN CONCENTRATORK063096PRECISION OXYGEN MONITOR

View all 29 devices →

Related Devices (Code: BZR)

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.

K243917F&P Optiflow Air/Oxygen Flow SourceFisher & Paykel Healthcare, Ltd.K241465Midas Flowmeter; eAVSParker Hannifin CorporationK231895Maxtec MaxBlend2+pMaxtec, LLCK230987FlowStar Analog Mixer FlowmeterBaldus Sedation GmbH & Co. KGK222794FlowStar Touch Digital Mixer FlowmeterBaldus Sedation GmbH & Co. KGK221494Quality Mix Blender, OxymixerDehas Medical Systems GmbH

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.

↑