Coopersurgical Digital Colposcopy System
FDA 510(k) K972630 · CooperSurgical, Inc.
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
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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| K182764 | Biop Digital ColposcopeHEX · Traditional | Biop Medical , Ltd. | 11/27/2018SE |
| K181034 | Pocket Colposcope SystemHEX · Traditional | Hadleigh Health Technologies, LLC | 09/21/2018SE |
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| K161871 | EVA (Enhanced Visual Assessment) SystemHEX · Traditional | Mobileodt , Ltd. | 12/19/2016SE |
| K160341 | Colposcope SystemHEX · Traditional | Xuzhou Kernel Medical Equipment Co., Ltd. | 09/14/2016SE |
| K160380 | LT-300 HDHEX · Traditional | Lutech Industries, Inc. | 05/13/2016SE |
| K151878 | Video ColposcopeHEX · Traditional | Edan Instruments, Inc. | 12/01/2015SE |
| K143119 | LT-300 Video ColposcopeHEX · Traditional | Lutech Industries, Inc. | 12/18/2014SE |
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| K250438 | CooperSurgical Milex® PessariesHHW · Traditional | 04/11/2025SE |
| K223064 | ALLY II Uterine Positioning System (UPS)LKF · Special | 10/28/2022SE |
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| K200038 | Endosee SystemHIH · Special | 02/05/2020SE |
| K191020 | G210 InviCell Plus with SignipHy pH monitoringPUB · Traditional | 01/14/2020SE |
| K191291 | Wallace Dual Lumen Oocyte Recovery SystemMQE · Special | 06/12/2019SE |
| K190639 | Endosee SystemHIH · Special | 05/15/2019SE |
| K182959 | Wallace Dual Lumen Oocyte Recovery SystemMQE · Traditional | 05/10/2019SE |
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.