Anarobe Systems
Mchenry, IL, US
Anarobe Systems appears in FDA device records in Mchenry, IL. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Anarobe Systems in 1984.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 7 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K842854 | MUELLER HINTON BROTH | JTZ | Substantially Equivalent | |
| K842850 | TRIPLE SUGAR IRON | JSH | Substantially Equivalent | |
| K842851 | ORNITHINE INDOLE MOTILITY | JSH | Substantially Equivalent | |
| K842855 | CHRISTENSEN'S UREA AGAR | JSF | Substantially Equivalent | |
| K842853 | LYSINE IRON AGAR | JSF | Substantially Equivalent | |
| K842852 | BRAIN HEART INFUSION BROTH | JSC | Substantially Equivalent | |
| K842849 | TRYPTICASE SOY BROTH | JSC | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain