Marion Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 38 products
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Total Devices38
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K883391 | POLYMER ADHESIVE BANDAGE | NAD | 1989-03-23 | View |
| 510(k) | K875182 | MODIFIED LABELING FOR TOXI-LAB THC SCREEN | DKE | 1988-07-05 | View |
| 510(k) | K875181 | MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM | 1988-05-27 | View | |
| 510(k) | K874554 | ENVICLUSIVE (TM) | NAD | 1988-03-11 | View |
| 510(k) | K874551 | ENVINET(TM) | EFQ | 1988-01-22 | View |
| 510(k) | K874552 | ENVISAN PAD | KOZ | 1988-01-22 | View |
| 510(k) | K874553 | ENVISAN PASTE | KOZ | 1987-12-18 | View |
| 510(k) | K870864 | CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST | LLH | 1987-04-14 | View |
| 510(k) | K863485 | MODIFICATION OF CDT(TM) CLOSTRIDIUM TEST | LLH | 1986-09-17 | View |
| 510(k) | K862123 | BIOSPHERE ANAEROBIC ENVIRONMENTAL DEVICE | KZJ | 1986-06-16 | View |
| 510(k) | K853073 | CULTURETTE BRAND 10-MINUTE GROUP A STREP I.D. | GTZ | 1985-08-01 | View |
| 510(k) | K852044 | CULTURETTE BRAND RAPID LATEX TEST CLOSTRIDIUM TOXI | LLH | 1985-07-19 | View |
| 510(k) | K851399 | BAC-T-SCREEN | JXA | 1985-06-04 | View |
| 510(k) | K845008 | BIO-BAG ENVIRONMENTAL CHAMBER -TYPE A-MULTI-PLATE | KZJ | 1985-03-05 | View |
| 510(k) | K833917 | BAC-T-SCREEN | JTA | 1984-01-13 | View |
| 510(k) | K831456 | TOXI-LAB CANNABINOID THC SCREEN | DKE | 1983-06-30 | View |
| 510(k) | K830372 | ARTIMICROBIAL REMOVAL DEVICE | LJF | 1983-04-08 | View |
| 510(k) | K823850 | BAC-T-SCREEN BACTERIURIA DETECTION DEV | JXA | 1983-03-01 | View |
| 510(k) | K823523 | TOXI-LAB RAPID SCREEN | DKJ | 1983-01-14 | View |
| 510(k) | K822344 | ANTIMICROBIAL REMOVAL DEVICE (ARD) | LJF | 1982-08-25 | View |
No matching devices.
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