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FDA 510(k)

VACUPLUS TUBES WITH BRICK RED STOPPERS

K-Number: K924365 · 1992-12-28

ApplicantStarplex Scientific, Inc.
Decision Date1992-12-28
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VACUPLUS TUBES WITH BRICK RED STOPPERS is the device name listed in this FDA 510(k) record. The listed applicant is Starplex Scientific, Inc.. It received FDA 510(k) clearance on 1992-12-28 under 510(k) number K924365. 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 VACUPLUS TUBES WITH BRICK RED STOPPERS?

VACUPLUS TUBES WITH BRICK RED STOPPERS is a medical device that received FDA 510(k) clearance on 1992-12-28. The listed applicant is Starplex Scientific, Inc.. The 510(k) number is K924365.

When did VACUPLUS TUBES WITH BRICK RED STOPPERS receive FDA 510(k) clearance?

VACUPLUS TUBES WITH BRICK RED STOPPERS received FDA 510(k) clearance on 1992-12-28, under 510(k) number K924365.

Who is the listed applicant for VACUPLUS TUBES WITH BRICK RED STOPPERS?

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

What is the FDA product code for VACUPLUS TUBES WITH BRICK RED STOPPERS?

The FDA product code for VACUPLUS TUBES WITH BRICK RED STOPPERS is JKA.

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Other records listing Starplex Scientific, 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.

K032246MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEMK022388STARTOX DRUG OF ABUSE SCREENING TEST (4)K021006STARTOX DRUG OF ABUSE SCREENING TESTK962843MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEMK960997STARSWAB CULTURE COLLECTION AND TRANSPORT SYSTEMK944847KULTSURE/STARSWAB ANAEROBIC TRANSPORT SYSTEM

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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 CompanyK252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeBecton, Dickinson and CompanyK252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderBecton, Dickinson and CompanyK252040BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection TubesBecton, Dickinson and Company

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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