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

MEDRAD COUNTERPOISE SYSTEM

K Number: K944983 · Decision Nov 29, 1994
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
105
Review Days
49

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Basic Information

Device Name
MEDRAD COUNTERPOISE SYSTEM
K Number
K944983
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medrad, Inc.
Date Received
October 11, 1994
Decision Date
November 29, 1994
Product Code
JAK
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAK System, X-Ray, Tomography, Computed

Similar 510(k) Clearances

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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
K122916 JETSTREAM NAVITUS L SYSTEM JEYSTREAM NAVITUS SYSTEM JETSTREAM G3 SF SYSTEM JETSTREAM SF 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
Search all 105 clearances from Medrad, Inc. →