Endo C Brush

FDA 510(k) K882628 · Milex Products, Inc.

Substantially Equivalent

510(k) numberK882628

Submission

Device name
Endo C Brush
Applicant
Milex Products, Inc.
Chicago, IL, US
Received
June 27, 1988
Decision date
July 25, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HHT – Spatula, Cervical, Cytological
Device class
Class II (moderate risk)
Regulation
21 CFR 884.4530
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Endo C Brush cleared by the FDA?

Endo C Brush (K882628) received a 510(k) decision of Substantially Equivalent on July 25, 1988, 28 days after the submission was received.

What is the product code of K882628?

The FDA product code is HHT – Spatula, Cervical, Cytological, a Class II (moderate risk) device regulated under 21 CFR 884.4530.