VITAFLON PLUS/VASCULON
FDA 510(k) clearance K941417 · decided 1994-10-06
Clearance details
- K-number
- K941417
- Device name
- VITAFLON PLUS/VASCULON
- Applicant
- Hogan & Hartson
- Decision
- Substantially Equivalent
- Date received
- 1994-03-23
- Decision date
- 1994-10-06
- Days to decision
- 197 days
- Clearance type
- Traditional
- Product code
- FOZ
- Device class
- 2
- Regulation number
- 880.5200
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Hogan & Hartson
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.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.