Atlas FDA

MONITRAL S

FDA 510(k) clearance K861230 · decided 1986-04-25

Clearance details

K-number
K861230
Device name
MONITRAL S
Applicant
Hospal Medical Corp.
Decision
Substantially Equivalent
Date received
1986-04-01
Decision date
1986-04-25
Days to decision
24 days
Clearance type
Traditional
Product code
FKP
Device class
2
Regulation number
876.5820
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
East Brunswick, NJ, US
Third-party review
No
Expedited review
No

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WATERCHECK REAGENT STRIP FOR CHLORINE & PEROXIDE (K953854)Integrated Biomedical Technology, Inc.1996-03-11
BIOPURE DIALYSATE CONCENTRATE MIX SYST/CONCENTRATE (K930181)Fresenius USA, Inc.1995-11-29
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Recalls involving this device

No recalls on record reference this clearance.