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510(k) Data Aggregation
K Number
K120195Device Name
SAFETY SUBCUTANEOUS TISSUE INFUSION SET
Manufacturer
Date Cleared
2012-07-06
(165 days)
Regulation Number
880.5440Why did this record match?
Applicant Name (Manufacturer) :
MULTI MED
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Safety Subcutaneous Infusion Set is designed specifically for the delivery of medications to the subcutaneous tissue.
Device Description
The safety subcutaneous needle infusion set consists of a sterile packaged kit including the infusion set and an adhesive dressing to hold the device in place. The unique Single, Bifurcated, Trifurcated, Quadfurcated, 5 and 6 Lumen for the Sub-Q have a luer lock at one end and a 90 degree needle mounted to a butterfly stabilizer at the other end. The sets are convenient to use, associated with less trauma, and offer an opportunity to improve compliance cost-effectively through the use of a dedicated infusion set. The device is for single use only.
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K Number
K002425Device Name
MEDIADENT HDX/MMD HDX SP XRAY SENSOR
Manufacturer
Date Cleared
2000-12-21
(135 days)
Product Code
Regulation Number
872.1800Why did this record match?
Applicant Name (Manufacturer) :
MULTI MEDIA DENTAL SYSTEMS, INC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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