The following data is part of a premarket notification filed by Dsp Worldwide with the FDA for Dermtome Blade.
| Device ID | K962371 |
| 510k Number | K962371 |
| Device Name: | DERMTOME BLADE |
| Classification | Dermatome |
| Applicant | DSP WORLDWIDE 49 PLAIN ST. North Attleboro, MA 02760 |
| Contact | Rosina Robinson |
| Correspondent | Rosina Robinson DSP WORLDWIDE 49 PLAIN ST. North Attleboro, MA 02760 |
| Product Code | GFD |
| CFR Regulation Number | 878.4820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-19 |
| Decision Date | 1996-08-29 |
| Summary: | summary |