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

DRS 4 DIALYZER REPROCESSING SYSTEM

K Number: K931336 · Decision Apr 18, 1996
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
56
Applicant Total
21
Review Days
1129

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Basic Information

Device Name
DRS 4 DIALYZER REPROCESSING SYSTEM
K Number
K931336
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Seratronics, Inc.
Date Received
March 16, 1993
Decision Date
April 18, 1996
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 Seratronics, Inc.

K Number Device Name
K955299 DPS 4 DIALYZER PREPARATION SYSTEM
K944539 DRS 4 ND DIALYZER REPROCESSING SYSTEM
K923529 DMS DATA MANAGEMENT SYSTEM/DRS-4 DIALYZER REPROCES
K914580 DRS-4 DIALYZER REPROCESSING SYSTEM
K874573 FRESENIUS PURISTERIL 340 (TM)
K874872 FRESENIUS HEMOFLOW F3, F4, F5, F7
K870725 FRESENIUS HEMOFLOW F6 AND F8
K870724 FRESENIUS HEMOFLOW F60 AND F80
K864587 FRESENIUS ULTRAFLUX AV400, AV600
K864169 FRESENIUS HEMOFLOW F50 & F70
Search all 21 clearances from Seratronics, Inc. →