The following data is part of a premarket notification filed by Bemis Health Care with the FDA for Suction Canister.
| Device ID | K771737 |
| 510k Number | K771737 |
| Device Name: | SUCTION CANISTER |
| Classification | Apparatus, Suction, Operating-room, Wall Vacuum Powered |
| Applicant | BEMIS HEALTH CARE 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GCX |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-09-15 |
| Decision Date | 1977-12-20 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00073088159533 | K771737 | 000 |
| 00073088159519 | K771737 | 000 |
| 10073088149210 | K771737 | 000 |
| 00073088159571 | K771737 | 000 |
| 10073088149548 | K771737 | 000 |