ELECTRO-CAUTERY KNIFE CLEANER 6000 1

Apparatus, Electrosurgical

DLP, INC.

The following data is part of a premarket notification filed by Dlp, Inc. with the FDA for Electro-cautery Knife Cleaner 6000 1.

Pre-market Notification Details

Device IDK852184
510k NumberK852184
Device Name:ELECTRO-CAUTERY KNIFE CLEANER 6000 1
ClassificationApparatus, Electrosurgical
Applicant DLP, INC. P.O.BOX 409 620 WATSONS S.W. Grand Rapids,  MI  49501
ContactRonald A Williams
CorrespondentRonald A Williams
DLP, INC. P.O.BOX 409 620 WATSONS S.W. Grand Rapids,  MI  49501
Product CodeHAM  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-05-20
Decision Date1985-06-04

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20613994698388 K852184 000

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