The following data is part of a premarket notification filed by Medical Wire & Equipment Company (bath) Ltd with the FDA for Virocult, Model Mw950.
| Device ID | K082472 |
| 510k Number | K082472 |
| Device Name: | VIROCULT, MODEL MW950 |
| Classification | Device, Specimen Collection |
| Applicant | MEDICAL WIRE & EQUIPMENT COMPANY (BATH) LTD POTLEY LANE Corsham, Wiltshire, GB Sn13 9rt |
| Contact | David Ellis |
| Correspondent | David Ellis MEDICAL WIRE & EQUIPMENT COMPANY (BATH) LTD POTLEY LANE Corsham, Wiltshire, GB Sn13 9rt |
| Product Code | LIO |
| CFR Regulation Number | 866.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-28 |
| Decision Date | 2008-12-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15060259076074 | K082472 | 000 |
| 25060259070512 | K082472 | 000 |
| 25060259070529 | K082472 | 000 |
| 25060259070536 | K082472 | 000 |
| 25060259070550 | K082472 | 000 |
| 25060259070567 | K082472 | 000 |
| 25060259072592 | K082472 | 000 |
| 25060259072608 | K082472 | 000 |
| 25060259072615 | K082472 | 000 |
| 25060259072707 | K082472 | 000 |
| 25060259074770 | K082472 | 000 |
| 25060259074817 | K082472 | 000 |
| 25060259074824 | K082472 | 000 |
| 25060259074831 | K082472 | 000 |
| 25060259070505 | K082472 | 000 |