NORFOLK MEDICAL PERITONEAL-ACCESS PORT
FDA 510(k) clearance K854593 · decided 1986-02-04
Clearance details
- K-number
- K854593
- Device name
- NORFOLK MEDICAL PERITONEAL-ACCESS PORT
- Applicant
- Norfolk Medical Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1985-11-18
- Decision date
- 1986-02-04
- Days to decision
- 78 days
- Clearance type
- Traditional
- Product code
- LMQ
- Device class
- 3
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Skokie, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Norfolk Medical Products
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Recalls involving this device
No recalls on record reference this clearance.