CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM
FDA 510(k) clearance K935092 · decided 1994-06-10
Clearance details
- K-number
- K935092
- Device name
- CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM
- Applicant
- Contour Fabricators of Florida, Inc.
- Decision
- Unknown
- Date received
- 1993-10-25
- Decision date
- 1994-06-10
- Days to decision
- 228 days
- Clearance type
- Traditional
- Product code
- FMF
- Device class
- 2
- Regulation number
- 880.5860
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- St. Petersburg, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.