FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)

K Number: K864267 · Decision Jan 9, 1987
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
15
Applicant Total
30
Review Days
72

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
SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)
K Number
K864267
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2260
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Millipore Corp.
Date Received
October 29, 1986
Decision Date
January 9, 1987
Product Code
DPM
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
DPM Columns, Liquid Chromatography

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DPM), 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
K934069 MILLEX, DUALEX (PLUS, ULTRA)
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
Search all 30 clearances from Millipore Corp. →