Laserscope Disposable Laparostat W/Irrig & Aspir

FDA 510(k) K912023 · Laserscope

Substantially Equivalent

510(k) numberK912023

Submission

Device name
Laserscope Disposable Laparostat W/Irrig & Aspir
Applicant
Laserscope
San Jose, CA, US
Received
May 7, 1991
Decision date
June 11, 1991
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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More from TroCare, LLC

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Questions and answers

When was Laserscope Disposable Laparostat W/Irrig & Aspir cleared by the FDA?

Laserscope Disposable Laparostat W/Irrig & Aspir (K912023) received a 510(k) decision of Substantially Equivalent on June 11, 1991, 35 days after the submission was received.

What is the product code of K912023?

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