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

HOSPAL TIPSTOP

K Number: K982818 · Decision Oct 21, 1998
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
221
Applicant Total
13
Review Days
71

Basic Information

Device Name
HOSPAL TIPSTOP
K Number
K982818
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GAMBRO HEALTHCARE
Date Received
August 11, 1998
Decision Date
October 21, 1998
Product Code
KMF
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KMF Bandage, Liquid

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Other Clearances by GAMBRO HEALTHCARE

K Number Device Name
K994390 GAMBRO POLYFLUX 17R, CAPILLARY DIALYZER/ FILTER
K990039 GAMBRO DQM 200
K982413 COBE ARYLANE H1, H4, H6 & H9 HEMODIALYZERS/FILTERS
K982414 GAMBRO POLYFLUX 11S, 14S, 17S & 21S HEMODIALYZERS/ HEMOFILTERS
K980386 HOSPAL MULTIFLOW 100, MULTIFLOW 100 KITS A0 (A0,A0/B AND A0/0), MULTIFLOW 100 KITS B22 (B22,B22/B, & B22/0)
K982760 COBE C HEMODIALYSIS DELIVERY SYSTEM , COBE CARTRIDGE BLOOD TUBING SET
K974899 GAMBRO CENTRAL WATER TREATMENT SYSTEM CWP 100 - WRO H
K981681 PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM)
K981085 GAMBRO HEMODIALYSIS WATER TREATMENT SYSTEM
K970253 COBE CENTRYSYSTEM 3 DIALYSIS CONTROL UNIT/COBE CARTRIDGE BLOOD TUBING SET
Search all 13 clearances from GAMBRO HEALTHCARE →