The following data is part of a premarket notification filed by Pryor Products with the FDA for Wheelchair Pal.
Device ID | K820964 |
510k Number | K820964 |
Device Name: | WHEELCHAIR PAL |
Classification | Accessories, Wheelchair |
Applicant | PRYOR PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KNO |
CFR Regulation Number | 890.3910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-04-06 |
Decision Date | 1982-04-16 |