The following data is part of a premarket notification filed by Inman Liebelt Corp. with the FDA for Ilc Forceps Pads.
| Device ID | K905583 |
| 510k Number | K905583 |
| Device Name: | ILC FORCEPS PADS |
| Classification | Forceps, Obstetrical |
| Applicant | INMAN LIEBELT CORP. P.O.BOX 171077 Arlington, TX 76003 |
| Contact | Roger Liebelt |
| Correspondent | Roger Liebelt INMAN LIEBELT CORP. P.O.BOX 171077 Arlington, TX 76003 |
| Product Code | HDA |
| CFR Regulation Number | 884.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-12 |
| Decision Date | 1991-04-12 |