Atlas FDA

WAKO(TM) PRETEST 5A

FDA 510(k) clearance K873366 · decided 1988-01-21

Clearance details

K-number
K873366
Device name
WAKO(TM) PRETEST 5A
Applicant
Wako Chemicals USA, Inc.
Decision
Substantially Equivalent
Date received
1987-08-21
Decision date
1988-01-21
Days to decision
153 days
Clearance type
Traditional
Product code
CDM
Device class
1
Regulation number
862.1785
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Dallas, TX, 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
URITEST 10 URINALYSIS REAGENT STRIPS (K052719)Arj Medical, Inc.2006-12-05
ACON URINALYSIS REAGENT STRIPS (K061559)Acon Laboratories Co.2006-08-11
URI-CHEM(R) GK,2,3,4C,5CN,6C,7C AND 8C (K880584)Mach Diag. C/O Wichita State University1988-05-31
TEST UROBILINOGEN IN URINE & LEUKOCYTES IN URINE (K852611)Miles Laboratories, Inc.1985-09-03
FITKIT I CHECKUP KIT (K821799)Patton, Boggs & Blow1983-08-16
FITKIT I CHECKUP KIT (K830340)Boditestor1983-08-16
DIA STRIPS SYSTEM (K831623)California Immuno Diagnostic, Inc.1983-07-28
REAGENT STRIPS FOR URINALYSIS (K790965)Miles Laboratories, Inc.1979-06-28

Recalls involving this device

No recalls on record reference this clearance.