CENTRIA T3 UPTAKE TEST SET
FDA 510(k) clearance K791050 · decided 1979-06-15
Clearance details
- K-number
- K791050
- Device name
- CENTRIA T3 UPTAKE TEST SET
- Applicant
- Ventrex Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-06-06
- Decision date
- 1979-06-15
- Days to decision
- 9 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Ventrex Laboratories
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.