Endoscopic Cable Drape

FDA 510(k) K931706 · Mayaguez Medical Center

Substantially Equivalent

510(k) numberK931706

Submission

Device name
Endoscopic Cable Drape
Applicant
Mayaguez Medical Center
Trophy Club, TX, US
Received
April 6, 1993
Decision date
August 6, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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More from TroCare, LLC

510(k)DeviceDecision
K93280510.0MM Suction/Irrigation Probe & Tubing KitGCJ · Traditional 08/16/1993SE
K932804Irrigating Tapered ProbeGCJ · Traditional 08/16/1993SE
K932806Poole Tip Suction Probe & Tubing KitGCJ · Traditional 08/11/1993SE
K931950Poole Tip Suction ProbeGCY · Traditional 08/11/1993SE
K931912Irrigating Blunt DissectorKYZ · Traditional 08/10/1993SE
K9318565.0 MM Irrigation/Aspiration ProbeGCY · Traditional 08/10/1993SE
K931854Endoscopic Blunt Dissecting InstrumentFGS · Traditional 08/10/1993SE
K931707Endoscopic Cable/Wire CoverGCJ · Traditional 08/06/1993SE
K931705Endoscopic Instrument HolderGCJ · Traditional 07/22/1993SE

Questions and answers

When was Endoscopic Cable Drape cleared by the FDA?

Endoscopic Cable Drape (K931706) received a 510(k) decision of Substantially Equivalent on August 6, 1993, 122 days after the submission was received.

What is the product code of K931706?

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