Atlas FDA

HYCEL DILUTOR, VARIOUS MODELS/MULTI

FDA 510(k) clearance K842747 · decided 1984-10-01

Clearance details

K-number
K842747
Device name
HYCEL DILUTOR, VARIOUS MODELS/MULTI
Applicant
R&D Systems, Inc.
Decision
Substantially Equivalent
Date received
1984-07-13
Decision date
1984-10-01
Days to decision
80 days
Clearance type
Traditional
Product code
GKH
Device class
1
Regulation number
864.5240
Medical specialty
Hematology
Advisory committee
Hematology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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COULTER CELLPREP (K021150)Beckman Coulter, Inc.2002-06-11
COULTER MULTI Q PREP (K935953)Coulter Corp.1994-03-11
COULTER MULTI-Q-PREP (K923530)Coulter Electronics, Inc.1992-10-14
FACSPREP ROBOTIC SAMPLE PREPARATION SYSTEM (K904795)Bd Becton Dickinson Vacutainer Systems Preanalytic1990-12-31
SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM (K882767)Toa Medical Electronics USA, Inc.1988-07-18
AD150, AUTOMATED HEMATOLOGY DILUTOR (K852373)Abbott Diagnostics1985-07-05
DILU-MATIC 140 (K842446)Abbott Diagnostics1984-09-06
DILULAB 230 (K823522)Innovative Medical Systems, Inc.1982-12-28
ROYCO MODEL 371 SUPER DILUTOR (K791644)Royco Instruments1979-09-19

Recalls involving this device

No recalls on record reference this clearance.