The following data is part of a premarket notification filed by Baylis Medical Co., Inc. with the FDA for Bmc Catheter Connector Cable, Model Rfp-101.
| Device ID | K023334 |
| 510k Number | K023334 |
| Device Name: | BMC CATHETER CONNECTOR CABLE, MODEL RFP-101 |
| Classification | Cable, Transducer And Electrode, Patient, (including Connector) |
| Applicant | BAYLIS MEDICAL CO., INC. 5160 EXPLORER DRIVE, UNIT 33 Mississauga, Ontario, CA L4w-4t7 |
| Contact | Amanda Hartley |
| Correspondent | Amanda Hartley BAYLIS MEDICAL CO., INC. 5160 EXPLORER DRIVE, UNIT 33 Mississauga, Ontario, CA L4w-4t7 |
| Product Code | DSA |
| CFR Regulation Number | 870.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-10-07 |
| Decision Date | 2002-12-31 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00685447000938 | K023334 | 000 |
| 00685447000921 | K023334 | 000 |
| 00685447000907 | K023334 | 000 |
| 00685447000891 | K023334 | 000 |
| 00685447000884 | K023334 | 000 |
| 00685447000877 | K023334 | 000 |
| 00685447004639 | K023334 | 000 |
| 00685447003960 | K023334 | 000 |
| 00685447005636 | K023334 | 000 |