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

MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT

K Number: K844850 · Decision Apr 2, 1985
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
60
Applicant Total
5
Review Days
110

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Basic Information

Device Name
MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT
K Number
K844850
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Medicorp, Inc.
Date Received
December 13, 1984
Decision Date
April 2, 1985
Product Code
FKQ
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
FKQ System, Dialysate Delivery, Central Multiple Patient

Similar 510(k) Clearances

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

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Other Clearances by Medicorp, Inc.

K Number Device Name
K860026 ULTRAMAX III, DIALYZER REPROCESSING DEVICE
K832705 ULTRAMAX
K791164 NEGATOVE PRESSURE CONVERTOR
K791396 MEDI-TRAK PORTABLE TRACTION DEVICE