Warner-Lambert Co.
FDA 510(k) & PMA Approved Devices — 50 products
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Total Devices50
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K024160 | NEOSPORIN SCAR SOLUTION | MDA | 2003-03-17 | View |
| 510(k) | K893452 | EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAM | IZZ | 1989-06-22 | View |
| 510(k) | K870584 | O.P.T.(TM) OVULATION PREDICTION TEST | CEP | 1987-11-25 | View |
| 510(k) | K861510 | MULTILUMEN VIAPIC CENTRAL LINE CATHETER | FOZ | 1986-06-09 | View |
| 510(k) | K852689 | GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK | JTN | 1985-08-19 | View |
| 510(k) | K852967 | GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISK | JTN | 1985-08-19 | View |
| 510(k) | K852843 | GENERAL DIAGNOSTICS COAG-A-MATE XC | KQC | 1985-08-13 | View |
| 510(k) | K852889 | GENERAL DIAGNOSTICS RAPID E. COLI TEST | JTO | 1985-07-23 | View |
| 510(k) | K850409 | GEN. DIAG. CHROMOSTRATE REF. PLASMA | JPA | 1985-05-08 | View |
| 510(k) | K850412 | GEN. DIAG. CHROMOSTRATE ANTITHROMBIN III ASSAY | JBQ | 1985-05-08 | View |
| 510(k) | K850410 | GEN. DIAG. CHROMOSTRATE PLASMINOGEN ASSAY | DDX | 1985-05-08 | View |
| 510(k) | K850411 | GEN. DIAG. CHROMOSTRATE ALPHA-2 ANTIPLASMIN ASSAY | LGP | 1985-05-08 | View |
| 510(k) | K850486 | GENERAL DIAG. CHROMOSTRATE HEPARIN ASSAY | KFF | 1985-05-08 | View |
| 510(k) | K850957 | GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK | JTN | 1985-05-01 | View |
| 510(k) | K851228 | GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISK | JTN | 1985-04-24 | View |
| 510(k) | K833369 | EARLY DETECTOR | KHE | 1984-08-02 | View |
| 510(k) | K833093 | VANISH II | KGO | 1983-12-12 | View |
| 510(k) | K833091 | DESERET SUBCLAVIAN JUGULAR CATH-SET | FOZ | 1983-11-21 | View |
| 510(k) | K833092 | DESERET ANGIO-GUIDE LARGE VEIN CATH. | FOZ | 1983-11-21 | View |
| 510(k) | K833352 | GEN. DIAGNOSTICS LOW FIBRINOGEN CONTROL | GIL | 1983-11-03 | View |
No matching devices.
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