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

CLINIC ELECTRONIC THERMOMETER

K Number: K850564 · Decision Feb 19, 1985
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
1
Review Days
7

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
CLINIC ELECTRONIC THERMOMETER
K Number
K850564
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Gemini Electronics Co. , Ltd.
Date Received
February 12, 1985
Decision Date
February 19, 1985
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FLL Continuous Measurement Thermometer

Similar 510(k) Clearances

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

View all