The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Corvac Blood Collection Tube.
| Device ID | K915213 |
| 510k Number | K915213 |
| Device Name: | CORVAC BLOOD COLLECTION TUBE |
| Classification | Tubes, Vacuum Sample, With Anticoagulant |
| Applicant | SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
| Contact | Dennis Pozzo |
| Correspondent | Dennis Pozzo SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
| Product Code | GIM |
| CFR Regulation Number | 862.1675 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-18 |
| Decision Date | 1992-01-08 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884527003164 | K915213 | 000 |
| 10884521742444 | K915213 | 000 |
| 10884521742420 | K915213 | 000 |
| 10884527003174 | K915213 | 000 |
| 30884527003185 | K915213 | 000 |
| 10884527003198 | K915213 | 000 |
| 10884527003204 | K915213 | 000 |
| 30884527003246 | K915213 | 000 |
| 30884527003253 | K915213 | 000 |
| 10884521742468 | K915213 | 000 |