Karl Storz Insulated Biopsy Forceps, Grasping/Dissecting Forecps, Flexible Forceps

FDA 510(k) K944765 · KARL STORZ Endoscopy-America, Inc.

Substantially Equivalent

510(k) numberK944765

Submission

Device name
Karl Storz Insulated Biopsy Forceps, Grasping/Dissecting Forecps, Flexible Forceps
Applicant
KARL STORZ Endoscopy-America, Inc.
Culver City, CA, US
Received
September 27, 1994
Decision date
March 28, 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
KGE – Forceps, Biopsy, Electric
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4300
Specialty
Gastroenterology, Urology

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Questions and answers

When was Karl Storz Insulated Biopsy Forceps, Grasping/Dissecting Forecps, Flexible Forceps cleared by the FDA?

Karl Storz Insulated Biopsy Forceps, Grasping/Dissecting Forecps, Flexible Forceps (K944765) received a 510(k) decision of Substantially Equivalent on March 28, 1995, 182 days after the submission was received.

What is the product code of K944765?

The FDA product code is KGE – Forceps, Biopsy, Electric, a Class II (moderate risk) device regulated under 21 CFR 876.4300.