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

FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G

K Number: K850127 · Decision Mar 20, 1985
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
56
Applicant Total
4
Review Days
65

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Basic Information

Device Name
FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G
K Number
K850127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Computer Dialysis Systems, Inc.
Date Received
January 14, 1985
Decision Date
March 20, 1985
Product Code
LIF
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
LIF Dialyzer Reprocessing System

Similar 510(k) Clearances

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

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Other Clearances by Computer Dialysis Systems, Inc.

K Number Device Name
K831132 COMPUDIAL/KP-1
K820575 J.E.T. DIALYSIS SYSTEM
K813107 COMPUDIAL/KP-1