510(k) K991754
- Device
- GO GLUCOSE MONITORING SYSTEM
- Applicant
- LXN CORP.
- 510(k) number
- K991754
- Product code
- CGA
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1999-09-08
- Date received
- 1999-05-24
- Regulation
- 862.1345
- Classification name
- Glucose Oxidase, Glucose
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Clearance type
- Traditional
- Third party reviewed
- No
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Legacy Summary#
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FDA Review#
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