FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Infrared Thermometer, model: PC808

K Number: K190717 · Decision Dec 13, 2019
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
2
Review Days
268

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
Infrared Thermometer, model: PC808
K Number
K190717
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shenzhen Pacom Medical Instruments Co., Ltd.
Date Received
March 20, 2019
Decision Date
December 13, 2019
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

Other Clearances by Shenzhen Pacom Medical Instruments Co., Ltd.

K Number Device Name
K172889 Infrared Thermometer