DOUBLE ANTIBODY BENZODIAZPINES #KBZD1, KBZD5
FDA 510(k) clearance K883459 · decided 1988-09-09
Clearance details
- K-number
- K883459
- Device name
- DOUBLE ANTIBODY BENZODIAZPINES #KBZD1, KBZD5
- Applicant
- Diagnostic Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 1988-08-12
- Decision date
- 1988-09-09
- Days to decision
- 28 days
- Clearance type
- Traditional
- Product code
- JXM
- Device class
- 2
- Regulation number
- 862.3170
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Los Angeles, CA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Diagnostic Products 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.
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.