Coopersurgical Digital Colposcopy System

FDA 510(k) K972630 · CooperSurgical, Inc.

Substantially Equivalent

510(k) numberK972630

Submission

Device name
Coopersurgical Digital Colposcopy System
Applicant
CooperSurgical, Inc.
North Attleboro, MA, US
Received
July 14, 1997
Decision date
February 2, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HEX – Colposcope (And Colpomicroscope)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1630
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Coopersurgical Digital Colposcopy System cleared by the FDA?

Coopersurgical Digital Colposcopy System (K972630) received a 510(k) decision of Substantially Equivalent on February 2, 1998, 203 days after the submission was received.

What is the product code of K972630?

The FDA product code is HEX – Colposcope (And Colpomicroscope), a Class II (moderate risk) device regulated under 21 CFR 884.1630.