The following data is part of a premarket notification filed by Medical Device Inspection Co., Inc. with the FDA for Powermatic Mat Platform.
| Device ID | K933578 |
| 510k Number | K933578 |
| Device Name: | POWERMATIC MAT PLATFORM |
| Classification | Table, Powered |
| Applicant | MEDICAL DEVICE INSPECTION CO., INC. 55 NORTHERN BLVD. SUITE 301 Great Neck, NY 11021 |
| Contact | Alan P Schwartz |
| Correspondent | Alan P Schwartz MEDICAL DEVICE INSPECTION CO., INC. 55 NORTHERN BLVD. SUITE 301 Great Neck, NY 11021 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-22 |
| Decision Date | 1993-11-05 |