FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VISION(R) PROTHROMBIN TIME

K Number: K883441 · Decision Sep 13, 1988
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
883
Review Days
29

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VISION(R) PROTHROMBIN TIME
K Number
K883441
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Abbott Laboratories
Date Received
August 15, 1988
Decision Date
September 13, 1988
Product Code
GJS
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GJS Test, Time, Prothrombin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GJS), ordered by most recent decision date.

View all

Other Clearances by Abbott Laboratories

K Number Device Name
K252424 Anti-HCV Next
K243500 ARCHITECT iGentamicin
K243168 Alinity i Rubella IgG
K243283 Alinity h-series System
K233932 Alinity i Toxo IgM
K232669 TBI
K222850 HAVAb IgG II
K220031 Alinity h-series System
K220282 i-STAT PTplus Cartridge with the i-STAT 1 System
K230937 Alinity i Total ß-hCG Reagent Kit, GLP systems Track
Search all 883 clearances from Abbott Laboratories →