The following data is part of a premarket notification filed by Baxa Corp., Sub. Of Cook Group, Inc. with the FDA for Baxa Tubing Sets (for Pharmacy Pump).
| Device ID | K872743 |
| 510k Number | K872743 |
| Device Name: | BAXA TUBING SETS (FOR PHARMACY PUMP) |
| Classification | Syringe, Piston |
| Applicant | BAXA CORP., SUB. OF COOK GROUP, INC. 13760 E. ARAPAHOE RD. Englewood, CO 80112 |
| Contact | Mary Steggall |
| Correspondent | Mary Steggall BAXA CORP., SUB. OF COOK GROUP, INC. 13760 E. ARAPAHOE RD. Englewood, CO 80112 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-07-13 |
| Decision Date | 1987-10-09 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50085412481406 | K872743 | 000 |
| 50085412476518 | K872743 | 000 |
| 50085412476570 | K872743 | 000 |
| 50085412476594 | K872743 | 000 |
| 50085412476822 | K872743 | 000 |
| 50085412476846 | K872743 | 000 |
| 50085412478321 | K872743 | 000 |
| 50085412478369 | K872743 | 000 |
| 50085412478376 | K872743 | 000 |
| 50085412480669 | K872743 | 000 |
| 55413765482590 | K872743 | 000 |