JERMYN OCCLUDERS KIT
FDA 510(k) clearance K830737 · decided 1983-06-02
Clearance details
- K-number
- K830737
- Device name
- JERMYN OCCLUDERS KIT
- Applicant
- Jermyn Specialties of California
- Decision
- Substantially Equivalent
- Date received
- 1983-03-08
- Decision date
- 1983-06-02
- Days to decision
- 86 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.