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 |