The following data is part of a premarket notification filed by Bemis Mfg. Co. with the FDA for Bemis One Quart Phlebotomy Container (part Number 100).
| Device ID | K960525 |
| 510k Number | K960525 |
| Device Name: | BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) |
| Classification | Container, Sharps |
| Applicant | BEMIS MFG. CO. 300 MILL ST. Sheboygan Falls, WI 53085 |
| Contact | John B Howell |
| Correspondent | John B Howell BEMIS MFG. CO. 300 MILL ST. Sheboygan Falls, WI 53085 |
| Product Code | MMK |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-02-05 |
| Decision Date | 1996-03-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10073088151923 | K960525 | 000 |
| 10073088148718 | K960525 | 000 |
| 10073088148725 | K960525 | 000 |
| 10073088148657 | K960525 | 000 |
| 10073088148640 | K960525 | 000 |