The following data is part of a premarket notification filed by Martin Medical with the FDA for Plaster Vacuum, 115v Model No. 4183-160.
| Device ID | K873721 |
| 510k Number | K873721 |
| Device Name: | PLASTER VACUUM, 115V MODEL NO. 4183-160 |
| Classification | Instrument, Cast Removal, Ac-powered |
| 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 | LGH |
| CFR Regulation Number | 888.5960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-09-15 |
| Decision Date | 1987-12-07 |