BLOOD CONTAINMENT PACK
FDA 510(k) clearance K872448 · decided 1987-11-17
Clearance details
- K-number
- K872448
- Device name
- BLOOD CONTAINMENT PACK
- Applicant
- Professional Medical Services
- Decision
- Substantially Equivalent
- Date received
- 1987-06-23
- Decision date
- 1987-11-17
- Days to decision
- 147 days
- Clearance type
- Traditional
- Product code
- LRO
- Device class
- 2
- Regulation number
- 878.4370
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- North Salt Lake, UT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.