510(k) K760743

Device
DONORMATIC (BLOOD COLLECTION DEVICE)
Applicant
Lifeline Instruments, Inc.
510(k) number
K760743
Product code
KSQ
Decision
Substantially Equivalent (SESE)
Decision date
1976-12-06
Date received
1976-09-30
Regulation
864.9195
Classification name
Device, Blood Mixing And Blood Weighing
Medical specialty
Hematology
Review panel
Hematology
Device class
1
Clearance type
Traditional
Third party reviewed
N

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KSQ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K842746HYCEL ROTOR-MIXER AND/OR MULTIR&D Systems, Inc.1984-08-17
K820712SEPCOR UNIT COLLECTION MONITORSeparation Science Corp.1982-05-07
K812533PLATELET AGITATORHelmer Labs, Inc.1981-09-29
K810617MOBILE MATIC AUTOMATIC DONOR SCALELifeline Instruments, Inc.1981-04-07
K802608HEMATIC BLOOD MIXERHelmer Labs, Inc.1980-12-11
K800104ROYCO MODEL 951 CELL MIXERRoyco Instruments1980-02-06
K780189PLATELET ROTATORTravenol Laboratories, S.A.1978-03-30