← Back to catalogue

Precision Xceed Pro

FDA UDI

Class I (US FDA UDI)

by Abbott Diabetes Care Inc

Identity

Trade Name
Precision Xceed Pro FDA UDI
Generic Name
Multiple clinical chemistry analyte monitoring system IVD, point-of-care FDA UDI
Device Name
Precision Xceed Pro Blood Glucose Test Strips FDA UDI
Model / Reference
70932 FDA UDI
Description
Precision Xceed Pro Blood Glucose Test Strips FDA UDI

Identifiers

Catalog Number
70932 FDA UDI
Primary DI / UDI-DI
00093815709329 FDA UDI
510(k) Number
K080960 FDA UDI
FDA Product Code
JIN FDA UDI
LFR FDA UDI
NBW FDA UDI
GMDN Term
Multiple clinical chemistry analyte monitoring system IVD, point-of-care FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1435 FDA UDI
862.1345 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple clinical chemistry analyte monitoring system IVD, point-of-care

Precision Xceed Pro by Abbott Diabetes Care Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple clinical chemistry analyte monitoring system IVD, point-of-care.

Cleared under the same submission

K080960 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Abbott Diabetes Care Inc

Sources (1)

  • FDA UDI 266e7cab-7e20-4284-9035-1b692b98be6a 37 fields · synced May 31, 2026