The following data is part of a premarket notification filed by Dlp, Inc. with the FDA for Electro-cautery Knife Cleaner 6000 1.
| Device ID | K852184 |
| 510k Number | K852184 |
| Device Name: | ELECTRO-CAUTERY KNIFE CLEANER 6000 1 |
| Classification | Apparatus, Electrosurgical |
| Applicant | DLP, INC. P.O.BOX 409 620 WATSONS S.W. Grand Rapids, MI 49501 |
| Contact | Ronald A Williams |
| Correspondent | Ronald A Williams DLP, INC. P.O.BOX 409 620 WATSONS S.W. Grand Rapids, MI 49501 |
| Product Code | HAM |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-05-20 |
| Decision Date | 1985-06-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20613994698388 | K852184 | 000 |