Cabot Medical-Surgitek Ultragold Plus Side-Firing Urologic Laser Fiber

FDA 510(k) K951714 · Cabot Medical Corp.

Substantially Equivalent

510(k) numberK951714

Submission

Device name
Cabot Medical-Surgitek Ultragold Plus Side-Firing Urologic Laser Fiber
Applicant
Cabot Medical Corp.
Langhorne, PA, US
Received
April 14, 1995
Decision date
July 11, 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
GEX – Powered Laser Surgical Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue, for general surgical purpose in medical specialties of general and plastic surgery, dermatology/aesthetic, podiatry, otolaryngology (ent), gynecology…

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Questions and answers

When was Cabot Medical-Surgitek Ultragold Plus Side-Firing Urologic Laser Fiber cleared by the FDA?

Cabot Medical-Surgitek Ultragold Plus Side-Firing Urologic Laser Fiber (K951714) received a 510(k) decision of Substantially Equivalent on July 11, 1995, 88 days after the submission was received.

What is the product code of K951714?

The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.