FDA 510(k) FDA class 2 Unknown 🇬🇧 United Kingdom

Rocket IPC Insertion Set, Rocket IPC Mini Insertion Set

K Number: K152105 · Decision Mar 29, 2016
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
14
Applicant Total
19
Review Days
244

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Basic Information

Device Name
Rocket IPC Insertion Set, Rocket IPC Mini Insertion Set
K Number
K152105
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Rocket Medical Plc
Date Received
July 29, 2015
Decision Date
March 29, 2016
Product Code
PNG
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PNG Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling

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Other 510(k) clearances with the same product code (PNG), ordered by most recent decision date.

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Other Clearances by Rocket Medical Plc

K Number Device Name
K210509 Rocket Platinum Cured Cathter
K163321 Rocket Indwelling Pleural Catheter (IPC) Insertion Kit
K162457 Rocket Indwelling Peritoneal Catheter (IPC) Insertion Kit
K123033 ROCKET IPC INSERTION PACK, ROCKET IPC MINI INSERTION SET, ROCKET IPC DRESSING PACK AND BOTTLE SET, ROCKET IPC DRAINAGE B
K052365 CERVINEEDLE DISPOSABLE CARTRIDGE SYRINGE
K042264 GUIDEWIRES
K040189 ENDOMETRIAL SAMPLING SYRINGE
K032015 EMBRYON ULTRASOUND NEEDLE GUIDE
K000205 EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES
K000340 HYSTALOG HSG CATHETER
Search all 19 clearances from Rocket Medical Plc →