The Karl Storz 26025UC Hamou Elec Hysteroflator

FDA 510(k) K912498 · KARL STORZ Endoscopy-America, Inc.

Substantially Equivalent

510(k) numberK912498

Submission

Device name
The Karl Storz 26025UC Hamou Elec Hysteroflator
Applicant
KARL STORZ Endoscopy-America, Inc.
Culver City, CA, US
Received
June 5, 1991
Decision date
December 18, 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
HIG – Insufflator, Hysteroscopic
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1700
Specialty
Obstetrics/Gynecology

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Questions and answers

When was The Karl Storz 26025UC Hamou Elec Hysteroflator cleared by the FDA?

The Karl Storz 26025UC Hamou Elec Hysteroflator (K912498) received a 510(k) decision of Substantially Equivalent on December 18, 1991, 196 days after the submission was received.

What is the product code of K912498?

The FDA product code is HIG – Insufflator, Hysteroscopic, a Class II (moderate risk) device regulated under 21 CFR 884.1700.