TROCAR CATHETER
FDA 510(k) clearance K851979 · decided 1985-06-17
Clearance details
- K-number
- K851979
- Device name
- TROCAR CATHETER
- Applicant
- Hospital Products Group
- Decision
- Substantially Equivalent
- Date received
- 1985-05-07
- Decision date
- 1985-06-17
- Days to decision
- 41 days
- Clearance type
- Traditional
- Product code
- JOL
- Device class
- 2
- Regulation number
- 880.6740
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Ny, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.