CORDIPAK ANGIOGRAPHY TRAY
FDA 510(k) clearance K863336 · decided 1986-09-12
Clearance details
- K-number
- K863336
- Device name
- CORDIPAK ANGIOGRAPHY TRAY
- Applicant
- Angi-Pak Corp.
- Decision
- Substantially Equivalent
- Date received
- 1986-08-28
- Decision date
- 1986-09-12
- Days to decision
- 15 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Miami, FL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Angi-Pak Corp.
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.