The following data is part of a premarket notification filed by Penox Technologies, Inc. with the FDA for Modified Penox Lift Chair.
| Device ID | K862654 |
| 510k Number | K862654 |
| Device Name: | MODIFIED PENOX LIFT CHAIR |
| Classification | Chair, Positioning, Electric |
| Applicant | PENOX TECHNOLOGIES, INC. ONE PENOX PLAZA, COMMERCE RD. P.O. BOX 785 Pittston, PA 18640 |
| Contact | Thana A France |
| Correspondent | Thana A France PENOX TECHNOLOGIES, INC. ONE PENOX PLAZA, COMMERCE RD. P.O. BOX 785 Pittston, PA 18640 |
| Product Code | INO |
| CFR Regulation Number | 890.3110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-07-11 |
| Decision Date | 1986-07-18 |