FDA UDI Not in Commercial Distribution 🇺🇸 United States

FloSense

DI: B279298010F1 · Model: KK · S D I DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
FloSense
Primary DI
B279298010F1
Version / Model
KK
Catalog Number
298010F
Company Name
S D I DIAGNOSTICS INC
Labeler DUNS
037690120
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2017-02-11
Public Version
4
Public Version Date
2019-08-26
Public Version Status
Update
Public Device Record Key
953fd021-2250-4b30-9e4d-017d364eca0f
Distribution End Date
2019-08-23

Device Description

Pneumotachometer

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JAX Pneumotachometer

GMDN Terms

Code Name
35282 Pulmonary function analysis system, adult

Identifiers

Type ID
Package B279298011F
Primary B279298010F1
Unit of Use B279298010F11

Premarket Submissions

Submission Number Supplement Number
K990962 000