GLUCOPRO SYRINGE, MODEL GPSY-XXXXXXXX
FDA 510(k) clearance K014114 · decided 2002-06-26
Clearance details
- K-number
- K014114
- Device name
- GLUCOPRO SYRINGE, MODEL GPSY-XXXXXXXX
- Applicant
- Nipro Diabetes Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2001-12-14
- Decision date
- 2002-06-26
- Days to decision
- 194 days
- Clearance type
- Traditional
- Product code
- FMF
- Device class
- 2
- Regulation number
- 880.5860
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Lexington, KY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.