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FILTER, EYRPUR DISPOSABLE LEUKOCITE

FDA 510(k) clearance K781803 · decided 1979-01-17

Clearance details

K-number
K781803
Device name
FILTER, EYRPUR DISPOSABLE LEUKOCITE
Applicant
Metrix Teknika, Inc.
Decision
Substantially Equivalent
Date received
1978-10-23
Decision date
1979-01-17
Days to decision
86 days
Clearance type
Traditional
Product code
GKT
Device class
2
Regulation number
864.9245
Medical specialty
Hematology
Advisory committee
Hematology
Location
MD, 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
AMICUS Separator System (K200530)Fresenius Kabi AG2020-09-11
AMICUS Separator System, AMICUS Separator System; Refurbished (K162462)Fresenius Kabi USA,Llc2016-11-23
AUTOMATED BLOOD CELL SEPARATOR (K822521)Cryosan, Inc.1982-09-30
AUTOMATED BLOOD CELL SEPAR. DISP. SFTWR (K820396)Pheragen Technology Corp.1982-04-27
CELLTRIFUGE II (K801233)Travenol Laboratories, S.A.1980-10-31
STERILE, DISPOSABLE CENTRIFUGE BOWL (K791106)Travenol Laboratories, S.A.1979-08-10
TERUMO IMUGARD (K790105)Terumo America, Inc.1979-05-24
BLOOD CELL SEPARATOR 2997 (K771258)Intl. Business Machines1977-09-06
BLOOD CELL PROCESSOR MODEL 2 IBM 2991 (K760856)Intl. Business Machines1977-01-10

Recalls involving this device

No recalls on record reference this clearance.