HOLLISTER MALE URINARY INCONT. SYSTEM
FDA 510(k) clearance K810708 · decided 1981-03-17
Clearance details
- K-number
- K810708
- Device name
- HOLLISTER MALE URINARY INCONT. SYSTEM
- Applicant
- Hollister, Inc.
- Decision
- Unknown
- Date received
- 1981-03-17
- Decision date
- 1981-03-17
- Days to decision
- 0 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.