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510(k) Data Aggregation
K Number
K960047Device Name
BRANNON PEDI PORTSYRINGE
Manufacturer
Date Cleared
1996-05-24
(143 days)
Product Code
Regulation Number
880.5860Why did this record match?
Applicant Name (Manufacturer) :
JAMES K. BRANNON
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
fluid aspiration and transfer of the fluid aspirate to vacuum specimen tubes and bottles
Device Description
The piston syringe, made available in a 3cc size, of this 510(k) notification, known as the Brannon Pedi PortSyringe (BPPS), is a combination of two legally marketed devices; (1) a piston syringe and (2) a blood specimen collection device (BSCD). The BSCD is integral with the plunger unit of the piston syringe with the BSCD communicating with the fluid chamber of the piston syringe via a centrally disposed and substantially narrow conduit. The fluid collection needle is sealed by a rubber sleeve. Appreciate that the needle is not manufactured by the applicant nor a manufacturing firm identified by the Applicant, but rather purchased from an FDA recognized manufacturer/distributor. Further appreciate that the BPPS is manufactured with identical material as the predicate piston syringe.
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K Number
K960049Device Name
BRANNON PORTSYRINGE
Manufacturer
Date Cleared
1996-05-24
(143 days)
Product Code
Regulation Number
880.5860Why did this record match?
Applicant Name (Manufacturer) :
JAMES K. BRANNON
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
fluid aspiration and transfer of the fluid aspirate to vacuum specimen tubes and bottles
Device Description
The piston syringe, made available in a 5cc size, of this 510(k) notification. known as the Brannon PortSyringe (BPS), is a combination of two legally marketed devices; (1) a piston syringe and (2) a blood specimen collection device (BSCD). The BSCD is integral with the plunger unit of the piston syringe with the BSCD communicating with the fluid chamber of the piston syringe via a centrally disposed and substantially narrow conduit. The fluid collection needle is sealed by a rubber sleeve. Appreciate that the needle is not manufactured by the applicant nor a manufacturing firm identified by the Applicant, but rather purchased from an FDA recognized manufacturer/distributor. Further appreciate that the BPS is manufactured with identical material as the predicate piston syringe.
Sealing of the conduit with the fluid collection needle allows the pistonplunger unit and the barrel to function as a conventional syringe. Functional operation simply requires that one compression fits a hypodermic needle of any gauge to the distal nozzle tip of the barrel. One is then able to aspirate body fluids as the predicate piston syringe. After a given amount of fluid is aspirated into the barrel of the syringe, a minimal amount will suffice, a plurality of vacuum specimen tubes can be inserted into the tube-holder. The vacuum specimen tubes are advanced over the sleeved needle while stabilizing the tube-holder. In so doing, the vacuum within the specimen tube induces the piston-plunger unit to advance distally as the aspirated fluid is transferred to the vacuum specimen tube proximally.
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