FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

ROCKET IPC INSERTION PACK, ROCKET IPC MINI INSERTION SET, ROCKET IPC DRESSING PACK AND BOTTLE SET, ROCKET IPC DRAINAGE B

K Number: K123033 · Decision Feb 1, 2013
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
18
Applicant Total
19
Review Days
126

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Basic Information

Device Name
ROCKET IPC INSERTION PACK, ROCKET IPC MINI INSERTION SET, ROCKET IPC DRESSING PACK AND BOTTLE SET, ROCKET IPC DRAINAGE B
K Number
K123033
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5050
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rocket Medical Plc
Date Received
September 28, 2012
Decision Date
February 1, 2013
Product Code
DWM
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DWM Apparatus, Suction, Patient Care

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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
K152105 Rocket IPC Insertion Set, Rocket IPC Mini Insertion Set
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
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