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510(k) Data Aggregation
K Number
K240514Device Name
AMT Low-Profile Suprapubic Catheter & Drainage Set
Manufacturer
Applied Medical Technology, Inc.
Date Cleared
2024-11-01
(253 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The AMT Low-Profile Suprapubic Catheter & Drainage Set is indicated for patients 7 years of age and older with lower urinary tract dysfunctions such as neurogenic bladder dysfunction or urethral obstruction or who are severely disabled or requiring constant care. The AMT Low-Profile Suprapubic Catheter & Drainage Set is indicated to be used for temporary suprapubic urinary diversion and drainage for less than or equal to four weeks. The AMT Low- Profile Suprapubic Catheter is intended to be placed directly into the bladder through a secured (initial placement) or formed (replacement) stoma.
Device Description
The Applied Medical Technology, Inc. (AMT) Low-Profile Suprapubic Catheter & Drainage Set (LPSPC) consists of two primary assemblies. The LPSPC is identical in materials and manufacturing processes to the Low-Profile Balloon Feeding Device cleared in K161413 for a different indication.
The Suprapubic Catheter is used to provide urinary diversion and drainage through the lower abdomen, placed and maintained in a percutaneously prepared cystostomy opening. The Drainage Set is intended to allow a connection between the suprapubic catheter device and a urinary collection bag system. The device is designed for bladder drainage by way of a secured (initial placement) or formed (replacement) cystostomy tract and may be used for irrigation. Patients may include: any user with urethral trauma, those who require long-term catheterization and urethral catheterization is intolerable, or those with a spinal cord injury and an inability to self-catheterize who may find the suprapubic method simpler to manage.
The LPSPC is a urinary drainage device made principally of silicone elastomer. The device consists of an internal retention balloon and a flexible external bolster with a balloon fill-valve, interlocking irrigation port, and safety plug. The catheter is inserted through the stoma and into the urinary bladder and is secured by the internal retention balloon. The device is offered in various sizes to accommodate different stoma diameters and lengths. On the shaft near the end is located a balloon which, when properly inflated, acts as an internal stabilizer preventing outward displacement through the stoma in the abdominal wall. The balloon is inflated through a separate inflation valve located in the external portion of the device.
The external profile of the device acts as a stabilizer to prevent inward migration and affords the user the ability to connect a provided Drainage Set.
The Drainage Set is identical in material and manufacturing process to certain configurations of the Irrigation Set included with the AMT Bowel Management Device previously cleared in K180026. The right-angle connector of the Drainage Set is compatible with the interlock on the LPSPC and is used to direct fluids drained from the bladder, through the catheter, and into a separate urinary collection bag.
The AMT Low-Profile Suprapubic Catheter & Drainage Set may optionally be marketed with a Foley Insertion Tray accessory. If included, the accessory would be a legally marketed Foley Insertion Tray, such as:
- AMSure Foley Insertion Tray (previously cleared Class II, Product Code FCM, K030664)
- Bardia Foley Insertion Tray (registered Class II, Product Code OHR, 510(k) exempt)
- Dynarex Foley insertion Tray without Catheter (registered Class II, Product Code OHR, 510(k) exempt)
The device is sold as sterile and can be initially placed in an outpatient-setting by a health care professional. The device may be replaced in an outpatient-setting or home setting by a health care professional or care giver.
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K Number
K181097Device Name
Cook Cystostomy Catheter Set
Manufacturer
Cook Incorporated
Date Cleared
2019-01-18
(267 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Cook® Cystostomy Catheter Set is used for temporary suprapubic urinary diversion and drainage for less than or equal to four weeks.
Device Description
The Cook® Cystostomy Catheter Set is composed of a single-lumen silicone catheter available in 8 to 12 French with a working length of 54 centimeters, a trocar stylet with access sheath having an outer diameter of 10 to 14 French with a length of either 11 or 11.2 centimeters, a drainage adapter with stopcock available in 12 to 16 gauge and a soft low-profile silicone catheter support with pull tie. The set is supplied sterile, intended for one-time use only, and packaged in a peelopen pouch with a three-year shelf life.
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K Number
K182709Device Name
One-Step Suprapubic Introducer
Manufacturer
Cook Incorporated
Date Cleared
2018-12-26
(90 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The One-Step Suprapubic Introducer is used for introducing a drainage catheter suprapubically into the bladder.
Device Description
The One-Step Suprapubic Introducer is comprised of a stainless steel trocar stylet needle and a dilator with a peel-away sheath. The trocar stylet needle is 20 centimeters (cm) long with a trocar beveled tip at the distal end of the device. The dilator is 14-22 French (Fr) and 18-19 cm in length. The peel-away sheath is 14-22 Fr and 17 cm in length. The three components are designed to fit together to form a single assembly.
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K Number
K182066Device Name
O'Brien Suprapubic Introducer Set, Cook SP Tube Introducer Set
Manufacturer
Cook Incorporated
Date Cleared
2018-10-30
(90 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The O'Brien Suprapubic Peel-Away Access Set is used for introducing a drainage catheter suprapubically into the bladder.
The Cook® SP Tube Introducer Set is used for introducing a drainage catheter suprapubically into the bladder.
Device Description
The O'Brien Suprapubic Peel-Away Access Set includes a peel-away sheath, dilator, trocar needle and wire guide. The peel-away sheath is available in even-numbered French sizes ranging from 16.0 to 20.0 and measures 22 centimeters in length. Dual knobs allow the sheath, manufactured from thick wall radiopaque polytetrafluoroethylene material, to be peeled back and removed.
The Cook SP Tube Introducer Set is comprised of a 20 Fr sheath which is 15 cm in length, an introducer that fits within this sheath, two dilators, a wire guide and needle.
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K Number
K132890Device Name
SUPRAPUBIC CATHETER AND INTRODUCER SET
Manufacturer
MEDIPLUS LTD.
Date Cleared
2014-01-17
(123 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Suprapubic Catheter and Introducer Set is indicated for drainage of the bladder through a needle puncture or stab wound over the bladder. For use no greater than 29 days.
Device Description
Suprapubic catheters are Foley catheters that are placed with an introducer through a needle puncture or stab wound over the bladder to allow bladder irrigation and / or drainage of the bladder. They are available in two (2) tip styles, closed and open tip, The introducer kit includes a number of components including: Scalpel, Syringe, 18 gauge needle, Dilator and Peelable sheath, and Guidewire
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K Number
K120127Device Name
SWAN VALLEY MEDICAL TRANURETHRAL SUPRAPUBIC ENDO-CYSTOSTOMY (T-SPEC) SURGICAL SYSTEM
Manufacturer
SWAN VALLEY MEDICAL, INCORPORATED
Date Cleared
2012-10-26
(283 days)
Product Code
KOB, FEX
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Swan Valley Medical Transurethral Suprapubic endo-Cystostomy (T-SPeC®) Surgical System is intended for suprapubic bladder catheterization (cystostomy) and drainage. The catheter should not be allowed to remain indwelling for more than 29 days.
Device Description
The T-SPeCTM Surgical System is, in effect, a sterile suprapubic catheter and accessory kit consisting of a) a suprapubic catheter; b) a catheter punch instrument used to create a cystostomy and place the suprapubic catheter; and c) a piston syringe to fill the catheter balloon after placement.
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K Number
K014002Device Name
ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890
Manufacturer
FORTUNE MEDICAL INSTRUMENT CORP.
Date Cleared
2002-03-04
(90 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Suprapubic Catheter is intended to use for drainage of the bladder through a needle puncture or stab wound over the bladder.
Device Description
Not Found
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K Number
K012153Device Name
LOWSLEY SUPRAPUBIC TRACTOR
Manufacturer
CIRCON VIDEO
Date Cleared
2001-09-19
(70 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The intended use for the Circon Lowsley™ Suprapubic Tractor is for conventional Open Perineal Prostatectomy Procedures and for Suprapubic Catheter Placement.
Device Description
Not Found
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K Number
K970969Device Name
KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
Manufacturer
THE KENDAL CO.
Date Cleared
1997-04-23
(37 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Kendall CURITY Suprapubic Catheter Trays and kits are intended to provide urinary bladder drainage or irrigation by percutaneous placement of a suprapubic catheter. This is a useful method of controlling urinary bladder drainage postoperatively.
Device Description
The Kendall Suprapubic Catheter Trays and Kits are sterile, single use devices which are designed to provide suprapubic access to the bladder for bladder irrigation and urine drainage. The proposed device consists of 100% silicone suprapubic catheters in 10, 12 and 14 French sizes packaged with various accessories.
The catheters are two-way balloon catheters having a drainage and inflation lumen.
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K Number
K970021Device Name
RUSCH SUPRAPUBIC TRAY
Manufacturer
RUSCH, INC.
Date Cleared
1997-02-07
(35 days)
Product Code
KOB
Regulation Number
876.5090Why did this record match?
Product Code :
KOB
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The kit is used for percutaneous bladder drainage and to drain fluids to and from the urinary tract.
Device Description
The kit consists of two major components: silicone catheter and plastic introducer assembly, along with attachment tape to fix the catheter to the skin, if required, and an optional scalpel. The kit is used for percutaneous bladder drainage. There are two types of silicone catheters. The first comes equip with one pair of drainage eyes. The second type of silicone catheter comes with six drainage eves arranged in a pigtail shape.
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