Atlas FDA

SICKLE CELL REAGENT SET

FDA 510(k) clearance K860812 · decided 1986-04-11

Clearance details

K-number
K860812
Device name
SICKLE CELL REAGENT SET
Applicant
Michclone Associates, Inc.
Decision
Substantially Equivalent
Date received
1986-03-04
Decision date
1986-04-11
Days to decision
38 days
Clearance type
Traditional
Product code
GHM
Device class
2
Regulation number
864.7825
Medical specialty
Hematology
Advisory committee
Hematology
Location
Detroit, MI, 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
SICKLE-CHEX SOLUBILITY KIT (K023656)Streck Laboratories, Inc.2002-12-30
SICKLE-CHEX (K013316)Streck Laboratories, Inc.2001-11-06
SAS SICKLE CELL TEST (K960947)Sa Scientific, Inc.1996-07-01
HEMOCARD HEMOGLOBIN S (K911981)Isolab, Inc.1991-10-09
HEMOCARD-AS (K910430)Isolab, Inc.1991-04-15
THROMBOSCREEN JOSHUA HEMOGLOBIN S SCREENING KIT (K872217)Pacific Hemostasis1987-07-31
SICKLE CELL REAGENT SET (K860420)Sterling Diagnostics, Inc.1986-02-24
THROMBO SCREEN SICKLE CELL ASSAY SET (K854079)Pacific Hemostasis1985-10-31
SICKLING HEMOGLOBIN CONTROLS, NORMAL (K842152)Isolab, Inc.1984-09-09
SICKLE-HEME A/S HETEROZYGOUS CONTROL (K842955)Michclone Associates, Inc.1984-08-09
SICKLE CELL REAGENT SET (K842368)Livonia Diagnostics, Inc.1984-07-20
SICKLE-STAT HEMOGLOBIN S SCREEN KIT (K841272)Clinical Technology Corp.1984-04-13

Recalls involving this device

RecordFirmDate
Sickle Heme, Hemoglobin S Solubility For Qualitative Determination of Hemoglobin S Test; , recall (Z-1501-2012)MichClone Associates, Inc.2012-05-09
BioTron Sickle Cell Reagent Set, Screening test for the Presence of Hemoglobin S 2 x 100 m recall (Z-1502-2012)MichClone Associates, Inc.2012-05-09
Sickle- Scan Hemoglobin S Cell Reagent Set, Catalog No. 13-2101 100 Tests For the Determin recall (Z-1503-2012)MichClone Associates, Inc.2012-05-09