The following data is part of a premarket notification filed by Martin Medical with the FDA for American Orthopaedic Vacuum 0295-250.
| Device ID | K861073 |
| 510k Number | K861073 |
| Device Name: | AMERICAN ORTHOPAEDIC VACUUM 0295-250 |
| Classification | Component, Cast |
| Applicant | MARTIN MEDICAL 36270 W. 103RD ST. P.O. BOX 590 Desoto, KS 66018 |
| Contact | Randy Kilburn |
| Correspondent | Randy Kilburn MARTIN MEDICAL 36270 W. 103RD ST. P.O. BOX 590 Desoto, KS 66018 |
| Product Code | LGF |
| CFR Regulation Number | 888.5940 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-03-21 |
| Decision Date | 1986-03-28 |