FDA UDI In Commercial Distribution 🇺🇸 United States

KoKo, LLC

DI: 00852417003491 · Model: KoKo Px 3000 Pulmonary Function Testing System · Koko, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KoKo, LLC
Primary DI
00852417003491
Version / Model
KoKo Px 3000 Pulmonary Function Testing System
Catalog Number
PX3000
Company Name
Koko, LLC
Labeler DUNS
117528917
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-05
Public Version
1
Public Version Date
2020-12-14
Public Version Status
New
Public Device Record Key
d1e817b6-7956-4b8c-805d-996b5ef43278

Device Description

Spirometry, Diffusion Capacity, and Nitrogen Washout Lung Volumes Pulmonary Function Testing System. Performs pre/post drug Spirometry (FVC, SVC & MVV), Bronchial Challenge, Diffusion Capacity (using ATS/ERS 10-second breath-hold or 3-Equation no breath hold methods), Single Breath Lung Volumes including SVC, Multiple Breath Nitrogen Washout Lung Volumes, Maldistribution of Ventilation, Delta N2 & Closing Volume, and optional Maximum Pressures (MIP/MEP) tests.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZG Spirometer, Diagnostic

GMDN Terms

Code Name
35282 Pulmonary function analysis system, adult

Identifiers

Type ID
Primary 00852417003491

Premarket Submissions

Submission Number Supplement Number
K030917 000