The following data is part of a premarket notification filed by Becton, Dickinson And Company with the FDA for Bd Cathena Safety Iv Catheter.
| Device ID | K172506 |
| 510k Number | K172506 |
| Device Name: | BD Cathena Safety IV Catheter |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | Becton, Dickinson And Company 9450 South State Street Sandy, UT 84070 |
| Contact | Henry Boland |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2017-08-18 |
| Decision Date | 2017-09-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30382903916635 | K172506 | 000 |
| 30382903868118 | K172506 | 000 |
| 30382903868101 | K172506 | 000 |
| 30382903868095 | K172506 | 000 |
| 30382903868088 | K172506 | 000 |
| 30382903868071 | K172506 | 000 |
| 30382903868064 | K172506 | 000 |
| 30382903868057 | K172506 | 000 |
| 30382903868040 | K172506 | 000 |
| 30382903868033 | K172506 | 000 |
| 30382903868026 | K172506 | 000 |
| 30382903868125 | K172506 | 000 |
| 30382903868132 | K172506 | 000 |
| 30382903868149 | K172506 | 000 |
| 30382903916628 | K172506 | 000 |
| 30382903916611 | K172506 | 000 |
| 30382903916604 | K172506 | 000 |
| 30382903868217 | K172506 | 000 |
| 30382903868200 | K172506 | 000 |
| 30382903868194 | K172506 | 000 |
| 30382903868187 | K172506 | 000 |
| 30382903868170 | K172506 | 000 |
| 30382903868163 | K172506 | 000 |
| 30382903868156 | K172506 | 000 |
| 30382903868019 | K172506 | 000 |