The following data is part of a premarket notification filed by Plastafil, Inc. with the FDA for Soft-tissue Instrument.
| Device ID | K841622 |
| 510k Number | K841622 |
| Device Name: | SOFT-TISSUE INSTRUMENT |
| Classification | Passer |
| Applicant | PLASTAFIL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HWQ |
| CFR Regulation Number | 888.4540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-19 |
| Decision Date | 1984-07-11 |