SEAGER ELECTROEJACULATOR
FDA 510(k) clearance K962379 · decided 1997-09-18
Clearance details
- K-number
- K962379
- Device name
- SEAGER ELECTROEJACULATOR
- Applicant
- National Rehab Hospital
- Decision
- Substantially Equivalent
- Date received
- 1996-06-20
- Decision date
- 1997-09-18
- Days to decision
- 455 days
- Clearance type
- Traditional
- Product code
- LNL
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.