The following data is part of a premarket notification filed by Inman Liebelt Corp. with the FDA for Intravascular Catheter Securment Device.
| Device ID | K912211 |
| 510k Number | K912211 |
| Device Name: | INTRAVASCULAR CATHETER SECURMENT DEVICE |
| Classification | Device, Intravascular Catheter Securement |
| Applicant | INMAN LIEBELT CORP. P.O.BOX 171077 Arlington, TX 76003 |
| Contact | H.clay Wilson |
| Correspondent | H.clay Wilson INMAN LIEBELT CORP. P.O.BOX 171077 Arlington, TX 76003 |
| Product Code | KMK |
| CFR Regulation Number | 880.5210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-05-20 |
| Decision Date | 1991-08-09 |