The following data is part of a premarket notification filed by Convaid Products, Inc. with the FDA for Convaid Cruiser Cp4m.
| Device ID | K810676 |
| 510k Number | K810676 |
| Device Name: | CONVAID CRUISER CP4M |
| Classification | Stroller, Adaptive |
| Applicant | CONVAID PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LBE |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-03-12 |
| Decision Date | 1981-03-26 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10840117400747 | K810676 | 000 |
| 10840117401027 | K810676 | 000 |
| 10840117400761 | K810676 | 000 |
| 10840117400365 | K810676 | 000 |
| 10840117400358 | K810676 | 000 |
| 10840117400341 | K810676 | 000 |
| 10840117400129 | K810676 | 000 |
| 10840117400099 | K810676 | 000 |
| 10840117400082 | K810676 | 000 |
| 10840117400075 | K810676 | 000 |
| 10840117400044 | K810676 | 000 |
| 10840117400037 | K810676 | 000 |
| 10840117401034 | K810676 | 000 |
| 10840117401041 | K810676 | 000 |
| 10840117400235 | K810676 | 000 |
| 10840117405759 | K810676 | 000 |
| 10840117405742 | K810676 | 000 |
| 10840117405735 | K810676 | 000 |
| 10840117405728 | K810676 | 000 |
| 10840117405711 | K810676 | 000 |
| 10840117401959 | K810676 | 000 |
| 10840117401744 | K810676 | 000 |
| 10840117401492 | K810676 | 000 |
| 10840117401249 | K810676 | 000 |
| 10840117401072 | K810676 | 000 |
| 10840117400013 | K810676 | 000 |