Cleared Traditional

VALLEYLAB FORCE 300

K953195 · Valleylab, Inc. · General & Plastic Surgery

Aug 1995

Decision

42d

Days

Class 2

Risk

About This 510(k) Submission

K953195 is an FDA 510(k) clearance for the VALLEYLAB FORCE 300, a Electrosurgical, Cutting & Coagulation & Accessories (Class II — Special Controls, product code GEI), submitted by Valleylab, Inc. (Boulder, US). The FDA issued a Cleared decision on August 21, 1995, 42 days after receiving the submission on July 10, 1995. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4400.

Submission Details

510(k) Number	K953195 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 10, 1995
Decision Date	August 21, 1995
Days to Decision	42 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	Summary PDF

Device Classification

Product Code	GEI — Electrosurgical, Cutting & Coagulation & Accessories
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 878.4400
Definition	Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).