The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Bard Safe Sampling Device.
| Device ID | K925446 |
| 510k Number | K925446 |
| Device Name: | BARD SAFE SAMPLING DEVICE |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | C.R. BARD, INC. 8195 INDUSTRIAL BLVD. Covington, GA 30014 |
| Contact | Donna J Wilson |
| Correspondent | Donna J Wilson C.R. BARD, INC. 8195 INDUSTRIAL BLVD. Covington, GA 30014 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-28 |
| Decision Date | 1993-07-29 |