Atlas FDA

CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)

FDA 510(k) clearance K873304 · decided 1987-09-11

Clearance details

K-number
K873304
Device name
CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)
Applicant
Miles Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1987-08-18
Decision date
1987-09-11
Days to decision
24 days
Clearance type
Traditional
Product code
LJX
Device class
1
Regulation number
864.7675
Medical specialty
Hematology
Advisory committee
Hematology
Location
Elkhart, IN, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Miles Laboratories

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
Healgen URS Test Strips (K231045)Healgen Scientific,, LLC2023-06-16
ACON UTI URINARY TRACT INFECTION TEST STRIPS (K063295)ACON Laboratories, Inc.2007-10-12
SERIM LEUKOCYTE ESTERASE TEST STRIPS (K000578)Serim Research Corp.2000-05-05
DIASCREEN REAGENT STRIPS (K981555)Chronimed, Inc.1998-06-01
DIASCREEN REAGENT STRIPS (K971976)Dia-Screen Corp.1997-06-17
LEUKOSTIX REAGENT STRIPS FOR URINALYSIS (K843727)Miles Laboratories, Inc.1985-01-04

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BIOSTATOR GLUCOSE CONTROLLER (P800032/S001)Miles Laboratories, Inc.1983-06-02
BIOSTATOR GLUCOSE CONTROLLER (P800032)Miles Laboratories, Inc.1981-05-28