The following data is part of a premarket notification filed by Suncoast Medical Manufacturers, Inc. with the FDA for Replace-a-tip Recharg. Low Temp..
Device ID | K841325 |
510k Number | K841325 |
Device Name: | REPLACE-A-TIP RECHARG. LOW TEMP. |
Classification | Unit, Cautery, Thermal, Battery-powered |
Applicant | SUNCOAST MEDICAL MANUFACTURERS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | HQP |
CFR Regulation Number | 886.4115 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-04-02 |
Decision Date | 1984-05-09 |