GLUCOSITE TEST SYSTEM
FDA 510(k) clearance K971145 · decided 1997-09-17
Clearance details
- K-number
- K971145
- Device name
- GLUCOSITE TEST SYSTEM
- Applicant
- Gds Technology, LLC
- Decision
- Substantially Equivalent
- Date received
- 1997-03-28
- Decision date
- 1997-09-17
- Days to decision
- 173 days
- Clearance type
- Traditional
- Product code
- CGA
- Device class
- 2
- Regulation number
- 862.1345
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Elkhart, IN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.