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

MAMMO M

K Number: K882133 · Decision Sep 19, 1988
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
16
Review Days
122

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Basic Information

Device Name
MAMMO M
K Number
K882133
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Ziehm International, Inc.
Date Received
May 20, 1988
Decision Date
September 19, 1988
Product Code
IZH
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
IZH System, X-Ray, Mammographic

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K894021 MOBILE X-RAY UNIT
K894041 PUMP-JECT SYRINGE WITH LUER-LOCK
K890620 STICK-GARD SAFETY NEEDLE
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. →