PORT-LOCK
FDA 510(k) clearance K823845 · decided 1983-03-01
Clearance details
- K-number
- K823845
- Device name
- PORT-LOCK
- Applicant
- Norfolk Medical Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-12-21
- Decision date
- 1983-03-01
- Days to decision
- 70 days
- Clearance type
- Traditional
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- 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.