Atlas FDA

DIASCREEN REAGENT STRIPS

FDA 510(k) clearance K981555 · decided 1998-06-01

Clearance details

K-number
K981555
Device name
DIASCREEN REAGENT STRIPS
Applicant
Chronimed, Inc.
Decision
Substantially Equivalent
Date received
1998-05-01
Decision date
1998-06-01
Days to decision
31 days
Clearance type
Traditional
Product code
LJX
Device class
1
Regulation number
864.7675
Medical specialty
Hematology
Advisory committee
Hematology
Location
Edina, MN, 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
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 (K971976)Dia-Screen Corp.1997-06-17
CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES) (K873304)Miles Laboratories, Inc.1987-09-11
LEUKOSTIX REAGENT STRIPS FOR URINALYSIS (K843727)Miles Laboratories, Inc.1985-01-04

Recalls involving this device

RecordFirmDate
Hypoguard, DiaScreen 4pH, Reagent Strips for Urinalysis, 100 strips, Cat. No. D11400. recall (Z-2634-2010)ARKRAY USA INC.2010-09-30