Inhealth Soft Sleeve Colonoscope Splint, Model CS1200

FDA 510(k) K023259 · Helix Medical, Inc.

Substantially Equivalent

510(k) numberK023259

Submission

Device name
Inhealth Soft Sleeve Colonoscope Splint, Model CS1200
Applicant
Helix Medical, Inc.
Carpinteria, CA, US
Received
September 30, 2002
Decision date
December 26, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FDF – Colonoscope And Accessories, Flexible/Rigid
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To examine or perform procedures in the colon or rectum For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was Inhealth Soft Sleeve Colonoscope Splint, Model CS1200 cleared by the FDA?

Inhealth Soft Sleeve Colonoscope Splint, Model CS1200 (K023259) received a 510(k) decision of Substantially Equivalent on December 26, 2002, 87 days after the submission was received.

What is the product code of K023259?

The FDA product code is FDF – Colonoscope And Accessories, Flexible/Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.