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

ZIEHM VISION

K Number: K011292 · Decision Jun 20, 2001
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
16
Review Days
51

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Basic Information

Device Name
ZIEHM VISION
K Number
K011292
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ziehm International, Inc.
Date Received
April 30, 2001
Decision Date
June 20, 2001
Product Code
OWB
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
OWB Interventional Fluoroscopic X-Ray System

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K894041 PUMP-JECT SYRINGE WITH LUER-LOCK
K890620 STICK-GARD SAFETY NEEDLE
K882133 MAMMO M
K843311 IV ADMIN. SET FOR MVP 1 INFUSION PUMP
K842263 MTP E.V. INFUSION PUMP
K831407 CARDIAC OUTPUT COMPUTER
K830453 IV ADMINISTRATION SETS - MVP INFUSION
Search all 16 clearances from Ziehm International, Inc. →