The following data is part of a premarket notification filed by Chase Medical, Inc. with the FDA for Chase Sucker.
| Device ID | K971022 |
| 510k Number | K971022 |
| Device Name: | CHASE SUCKER |
| Classification | Apparatus, Suction, Operating-room, Wall Vacuum Powered |
| Applicant | CHASE MEDICAL, INC. 1876 FIRMAN DR. Richardson, TX 75081 |
| Contact | Bert Davis |
| Correspondent | Bert Davis CHASE MEDICAL, INC. 1876 FIRMAN DR. Richardson, TX 75081 |
| Product Code | GCX |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-03-20 |
| Decision Date | 1997-04-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10817278012676 | K971022 | 000 |
| 10817278010511 | K971022 | 000 |
| 10817278010528 | K971022 | 000 |
| 10817278011273 | K971022 | 000 |
| 10817278011280 | K971022 | 000 |
| 10817278011396 | K971022 | 000 |
| 10817278011457 | K971022 | 000 |
| 10817278011464 | K971022 | 000 |
| 20817278011751 | K971022 | 000 |
| 10817278012492 | K971022 | 000 |
| 10817278010504 | K971022 | 000 |