Microsurge Thoracoscopic Access System

FDA 510(k) K953121 · Microsurge, Inc.

Substantially Equivalent

510(k) numberK953121

Submission

Device name
Microsurge Thoracoscopic Access System
Applicant
Microsurge, Inc.
Needham, MA, US
Received
July 5, 1995
Decision date
September 29, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

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).

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K954641Endo-LeaderOCW · Traditional 12/28/1995SE
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K933750Microsurge Reusable Front End Grasp Devices, ModifGCJ · Traditional 06/10/1994SE
K930355Microsurge Suction/Irrigation System CannulasGEI · Traditional 06/08/1993SE
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Questions and answers

When was Microsurge Thoracoscopic Access System cleared by the FDA?

Microsurge Thoracoscopic Access System (K953121) received a 510(k) decision of Substantially Equivalent on September 29, 1995, 86 days after the submission was received.

What is the product code of K953121?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.