STERILE PROCEDURAL TRAYS
FDA 510(k) clearance K870373 · decided 1987-03-20
Clearance details
- K-number
- K870373
- Device name
- STERILE PROCEDURAL TRAYS
- Applicant
- Dimed, Intl.
- Decision
- Unknown
- Date received
- 1987-01-29
- Decision date
- 1987-03-20
- Days to decision
- 50 days
- Clearance type
- Traditional
- Product code
- KDD
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Plant City, FL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.