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

JETSTREAM NAVITUS L SYSTEM JEYSTREAM NAVITUS SYSTEM JETSTREAM G3 SF SYSTEM JETSTREAM SF 1.6 SYSTEM

K Number: K122916 · Decision Oct 19, 2012
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
145
Applicant Total
105
Review Days
28

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Basic Information

Device Name
JETSTREAM NAVITUS L SYSTEM JEYSTREAM NAVITUS SYSTEM JETSTREAM G3 SF SYSTEM JETSTREAM SF 1.6 SYSTEM
K Number
K122916
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medrad, Inc.
Date Received
September 21, 2012
Decision Date
October 19, 2012
Product Code
MCW
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
MCW Catheter, Peripheral, Atherectomy

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Other Clearances by Medrad, Inc.

K Number Device Name
K133023 JETSTREAM XC 2.4/3.4; JETSTREAM XC 2.1/3.0; JETSTREAM SC 1.85; JETSTREAM SC 1.6
K130381 ANGIOJET ULTRA POWER PULSE KIT
K130637 JETSTREAM XC 2.4/3.4 SYSTEM; JETSTREAM XC 2.1/3.0 SYSTEM; JETSTREAM SC 1.85 SYSTEM; JETSTREAM SC 1.6 SYSTEM
K113363 ANGIOJET SOLENT DISTA THROMBECTOMY SET
K113133 MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM), (TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION ARTERION SYRINGE
K113428 ANGIOJET ULTRA DVX THROMBECTOMY SET
K112086 MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM / TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION SYRINGE
K111182 ANGIOJET SOLENT OMNI THROMBECTOMY SET
K100798 MEDRAD INTEGO PET INFUSION SYSTEM, SOURCE ADMINISTRATION SET, PATIENT ADMINSTRATIN SET MODEL INT SYS 100, INT CSS, INT C
K082905 MEDRAD STELLANT CT INJECTOR SYSTEM WITH P3T CARDIAC
Search all 105 clearances from Medrad, Inc. →