SEERAM BLADE
FDA 510(k) clearance K844073 · decided 1984-11-19
Clearance details
- K-number
- K844073
- Device name
- SEERAM BLADE
- Applicant
- Seeram Products Development
- Decision
- Substantially Equivalent
- Date received
- 1984-10-19
- Decision date
- 1984-11-19
- Days to decision
- 31 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Vero Beach, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.