Atlas FDA

POTASSIUM TEST

FDA 510(k) clearance K811661 · decided 1981-06-25

Clearance details

K-number
K811661
Device name
POTASSIUM TEST
Applicant
King Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1981-06-15
Decision date
1981-06-25
Days to decision
10 days
Clearance type
Traditional
Product code
CEJ
Device class
2
Regulation number
862.1600
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Walker, 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
POTASSIUM TEST KIT AND ELECTROLYTE CAL 1 AND 2 (K043267)Randox Laboratories, Ltd.2005-02-10
POTASSIUM QVET (K943026)Prisma Systems1994-12-09
REFLOTRON POTASSIUM TEST TABS (K904033)Boehringer Mannheim Corp.1990-11-06
POTASSIUM REAGENT SET (K902574)Tech-Co, Inc.1990-07-10
TECHNICON RA-100 SYSTEM POTASSIUM (K883586)Technicon Instruments Corp.1988-11-29
TECHNICON ASSIST POTASSIUM (K883585)Technicon Instruments Corp.1988-11-29
IQ POTASSIUM (K881440)Bd Becton Dickinson Vacutainer Systems Preanalytic1988-05-27
EASY-TEST POTASSIUM K ITEM NUMBER 19XXX (K880339)Em Diagnostic Systems, Inc.1988-02-25
POTASSIUM TEST (K863486)Sclavo, Inc.1986-09-29
SERUM POTASSIUM REAGENT SET (K861713)Sterling Diagnostics, Inc.1986-05-23
QCA POTASSIUM TEST KIT (K853404)Bd Becton Dickinson Vacutainer Systems Preanalytic1985-08-23
BCS POTASSIUM TURBIDIMETRIC TEST (K850258)Bioclinical Systems, Inc.1985-02-07

Recalls involving this device

No recalls on record reference this clearance.