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FDA 510(k)

DIFF SAFE

K-Number: K914129 · 1991-10-11

ApplicantMarshall Levinson
Decision Date1991-10-11
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIFF SAFE is the device name listed in this FDA 510(k) record. The listed applicant is Marshall Levinson. It received FDA 510(k) clearance on 1991-10-11 under 510(k) number K914129. 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 DIFF SAFE?

DIFF SAFE is a medical device that received FDA 510(k) clearance on 1991-10-11. The listed applicant is Marshall Levinson. The 510(k) number is K914129.

When did DIFF SAFE receive FDA 510(k) clearance?

DIFF SAFE received FDA 510(k) clearance on 1991-10-11, under 510(k) number K914129.

Who is the listed applicant for DIFF SAFE?

The FDA 510(k) record lists Marshall Levinson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIFF SAFE?

The FDA product code for DIFF SAFE is JKA.

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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