RE-CELL SLIDE RECAP
FDA 510(k) clearance K772139 · decided 1978-01-05
Clearance details
- K-number
- K772139
- Device name
- RE-CELL SLIDE RECAP
- Applicant
- Geometric Data, Div. Smithkline Corp.
- Decision
- Substantially Equivalent
- Date received
- 1977-11-14
- Decision date
- 1978-01-05
- Days to decision
- 52 days
- Clearance type
- Traditional
- Product code
- JOY
- Device class
- 2
- Regulation number
- 864.5260
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.