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FDA 510(k)

PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM

K-Number: K030076 · 2003-07-07

ApplicantBiomed Personal Metabolic and Nutritional Testing
Decision Date2003-07-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomed Personal Metabolic and Nutritional Testing. It received FDA 510(k) clearance on 2003-07-07 under 510(k) number K030076. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM?

PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-07. The listed applicant is Biomed Personal Metabolic and Nutritional Testing. The 510(k) number is K030076.

When did PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM receive FDA 510(k) clearance?

PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM received FDA 510(k) clearance on 2003-07-07, under 510(k) number K030076.

Who is the listed applicant for PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM?

The FDA 510(k) record lists Biomed Personal Metabolic and Nutritional Testing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM?

The FDA product code for PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM is JKA.

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.

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Other records listing Biomed Personal Metabolic and Nutritional Testing 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.

K030394FLUID SAMPLE RETRIEVAL SYSTEM

Related Devices (Code: JKA)

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.

K262215Profoject™ Safety Sliding Blood Collection SetCMT Health PTE., Ltd.K252899Female Culture Device; Male Culture Device; Transfer Device; Access DeviceZhejiang Kindly Medical Device Co., Ltd.K260128BD Preset™ and BD A-Line™ Arterial Blood Collection SyringesBecton, Dickinson and CompanyK252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderBecton, Dickinson and CompanyK252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeBecton, Dickinson and CompanyK252040BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection TubesBecton, Dickinson and Company

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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