Hyland Therapeutic Div., Travenol Laboratories
FDA 510(k) & PMA Approved Devices — 44 products
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Total Devices44
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K820835 | ALUMINA SILICA-ACTIVATED PARTIAL THROM | GFO | 1982-04-26 | View |
| 510(k) | K820192 | HAEMOPHILUS INFLUENZAE TYPE B ANTISERUM | GRP | 1982-03-11 | View |
| 510(k) | K812220 | NEPHELOMETRIC SOLID TURBIDITY STANDARD | JIW | 1981-08-18 | View |
| 510(k) | K810078 | Q-PAK THERAPEUTIC DRUG MONIT. CONTROL S | DIF | 1981-02-02 | View |
| 510(k) | K810077 | OMEGA THERAPEUTIC DRUG MONIT. CONTROL S. | DIF | 1981-01-28 | View |
| 510(k) | K802610 | ALERT A,HDL-APOLIPOROTEIN A, TEST KIT | DER | 1981-01-05 | View |
| 510(k) | K791113 | LOW IONIC STRENGTH SOLUTION (LISS) | KSG | 1979-06-28 | View |
| 510(k) | K790249 | TEST CELLS | KSF | 1979-05-16 | View |
| 510(k) | K781225 | GLOBULIN TEST, HUMAN THYROXINE BINDING | CEE | 1978-08-31 | View |
| 510(k) | K780962 | AUTOMATED ENZYME | KSK | 1978-07-27 | View |
| 510(k) | K780785 | DILUTOR TRANSPORTER | JQW | 1978-06-14 | View |
| 510(k) | K780753 | LAS-R HUMAN IGE TEST | DGC | 1978-06-06 | View |
| 510(k) | K780729 | LAS-R HUMAN COMPLEMENT CLQ TEST | DAK | 1978-05-18 | View |
| 510(k) | K780203 | THROMBOPLASTIN DRIED | GJS | 1978-03-27 | View |
| 510(k) | K780335 | LAS-R HUMAN C1 ESTERASE INHIBITOR TEST | DBA | 1978-03-22 | View |
| 510(k) | K780204 | CHEMISTRY CONTROL & REFERENCE SERUMS | JJT | 1978-03-03 | View |
| 510(k) | K772327 | LAS-R HUMAN IGD TEST | CZJ | 1978-02-28 | View |
| 510(k) | K772328 | LAS-R HUMAN ANTITHROMBIN III TEST | JBQ | 1978-02-03 | View |
| 510(k) | K772329 | LAS-R HUMAN PREALBUMIN TEST | JZJ | 1978-02-03 | View |
| 510(k) | K772085 | LAS-R HUMAN PLASMINOGEN TEST | DDX | 1978-01-24 | View |
No matching devices.
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