The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Blood Collection Tube, Lavender.
| Device ID | K771052 |
| 510k Number | K771052 |
| Device Name: | BLOOD COLLECTION TUBE, LAVENDER |
| Classification | Tubes, Vacuum Sample, With Anticoagulant |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GIM |
| CFR Regulation Number | 862.1675 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-06-13 |
| Decision Date | 1977-06-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884527006632 | K771052 | 000 |
| 20884527006615 | K771052 | 000 |
| 20884527006622 | K771052 | 000 |
| 20884527006646 | K771052 | 000 |
| 20884527006653 | K771052 | 000 |
| 20884527006660 | K771052 | 000 |
| 20884527006592 | K771052 | 000 |
| 10884521150638 | K771052 | 000 |
| 20884521150093 | K771052 | 000 |
| 20884527002990 | K771052 | 000 |