The following data is part of a premarket notification filed by Puritan Medical Products Llc with the FDA for Transport Culture Medium Device.
| Device ID | K120846 |
| 510k Number | K120846 |
| Device Name: | TRANSPORT CULTURE MEDIUM DEVICE |
| Classification | Device, Specimen Collection |
| Applicant | PURITAN MEDICAL PRODUCTS LLC 31 SCHOOL STREET P.O. BOX 149 Guilford, ME 04443 |
| Contact | Mehdi Karamchi |
| Correspondent | Mehdi Karamchi PURITAN MEDICAL PRODUCTS LLC 31 SCHOOL STREET P.O. BOX 149 Guilford, ME 04443 |
| Product Code | LIO |
| Subsequent Product Code | JTW |
| Subsequent Product Code | JTX |
| CFR Regulation Number | 866.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-03-20 |
| Decision Date | 2012-06-08 |
| Summary: | summary |