Atlas FDA

COTRAL I W/4.5 L/HR. ULTRAFILTRAT. CAPA

FDA 510(k) clearance K822386 · decided 1982-10-06

Clearance details

K-number
K822386
Device name
COTRAL I W/4.5 L/HR. ULTRAFILTRAT. CAPA
Applicant
Hospal Medical Corp.
Decision
Substantially Equivalent
Date received
1982-08-09
Decision date
1982-10-06
Days to decision
58 days
Clearance type
Traditional
Product code
FII
Device class
2
Regulation number
876.5860
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
NXSTAGE SYSTEM ONE (K030470)Nxstage Medical, Inc.2003-07-07
GAMBRO MULTIPURPOSE SYSTEM MPS-10 (K881270)Gambro, Inc.1988-08-24
HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309 (K872364)Travenol Laboratories, S.A.1987-10-13
HEMOFILTRATION SYSTEM 10 (K862716)Gambro, Inc.1986-09-09

Recalls involving this device

No recalls on record reference this clearance.