The following data is part of a premarket notification filed by Jeneric/pentron, Inc. with the FDA for Corrected-v.p.s..
| Device ID | K914178 |
| 510k Number | K914178 |
| Device Name: | CORRECTED-V.P.S. |
| Classification | Material, Impression |
| Applicant | JENERIC/PENTRON, INC. 53 N. PLAINS INDUSTRIAL RD. P.O. BOX 724 Wallingford, CT 06492 |
| Contact | Vincent Paradiso |
| Correspondent | Vincent Paradiso JENERIC/PENTRON, INC. 53 N. PLAINS INDUSTRIAL RD. P.O. BOX 724 Wallingford, CT 06492 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-18 |
| Decision Date | 1992-04-28 |