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

MILLEX, DUALEX (PLUS, ULTRA)

K Number: K934069 · Decision Apr 21, 1994
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
34
Applicant Total
30
Review Days
244

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MILLEX, DUALEX (PLUS, ULTRA)
K Number
K934069
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Millipore Corp.
Date Received
August 20, 1993
Decision Date
April 21, 1994
Product Code
FIB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FIB Protector, Transducer, Dialysis

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FIB), ordered by most recent decision date.

View all

Other Clearances by Millipore Corp.

K Number Device Name
K023892 MILLEX VV, GV, AND HV SYRINGE FILTER UNITS
K013988 MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R
K963717 MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)
K941326 ULTRAFREE-CL
K924347 WATERS(TM) 996 PDA
K922388 WATERS(TM) LC MODULE I FOR CLINICAL USE
K920136 WATERS 717 AUTOSAMPLER
K914841 CHROMATOGRAPHY CLINICAL USE 75JQR
K903647 MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE
K872792 WATERS M600E MULTI-SOLVENT DELIVERY SYSTEM
Search all 30 clearances from Millipore Corp. →