The following data is part of a premarket notification filed by Dittmar And Penn Corp. with the FDA for Dittmar Power Lifter.
| Device ID | K883260 |
| 510k Number | K883260 |
| Device Name: | DITTMAR POWER LIFTER |
| Classification | Stand, Infusion |
| Applicant | DITTMAR AND PENN CORP. 101 EAST LAUREL AVE. P.O. BOX 66 Cheltenham, PA 19012 -0066 |
| Contact | J. J Nowak |
| Correspondent | J. J Nowak DITTMAR AND PENN CORP. 101 EAST LAUREL AVE. P.O. BOX 66 Cheltenham, PA 19012 -0066 |
| Product Code | FOX |
| CFR Regulation Number | 880.6990 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-03 |
| Decision Date | 1988-11-07 |