FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IC-1545-DL MULTI FLO DVT COMBO INTERMITTENT PNEUMATIC COMPRESSION DEVICE

K Number: K131306 · Decision Jul 22, 2013
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
15
Review Days
76

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Basic Information

Device Name
IC-1545-DL MULTI FLO DVT COMBO INTERMITTENT PNEUMATIC COMPRESSION DEVICE
K Number
K131306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio Compression Systems, Inc.
Date Received
May 7, 2013
Decision Date
July 22, 2013
Product Code
JOW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
JOW Sleeve, Limb, Compressible

Similar 510(k) Clearances

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Other Clearances by Bio Compression Systems, Inc.

K Number Device Name
K250974 Bio Arterial Deluxe (IC-BAP-DX)
K213533 Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL, SC-4008-DL
K210417 Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL, SC-4008-DL
K180248 VascuEase IC-1200-WH
K171793 Sequential Circulator SC-2004FC-OC
K150953 Sequential Circulator SC-2008-OC, Sequential Circulator SC-2004-OC
K142640 Model SC-3004-DL Sequential Circulator, Model SC-3004FC-DL Sequenstial Circulator, Model SC-2008-DL Sequential Circulator, Model SC-3008-DL Sequential Circulator
K131327 BIOARTERIAL PLUS ARTERIAL BLOOD FLOW ENHANCEMENT SYSTEM
K122112 2004-OC MASSAGE SYSTEM, 2008-OC MASSAGE SYSTEM
K072666 BIOARTERIAL PLUS, ARTERIAL BLOOD FLOW ENHANCEMENT SYSTEM
Search all 15 clearances from Bio Compression Systems, Inc. →