Dynatech JD7/JD7P Colposcope

FDA 510(k) K761205 · Dynatech Cryomedical Co.

Substantially Equivalent

510(k) numberK761205

Submission

Device name
Dynatech JD7/JD7P Colposcope
Applicant
Dynatech Cryomedical Co.
Mchenry, IL, US
Received
December 7, 1976
Decision date
December 17, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K182764Biop Digital ColposcopeHEX · Traditional Biop Medical , Ltd.11/27/2018SE
K181034Pocket Colposcope SystemHEX · Traditional Hadleigh Health Technologies, LLC09/21/2018SE
K170446LT-300 SD Digital Video ColposcopeHEX · Traditional Lutech Industries, Inc.05/21/2017SE
K161871EVA (Enhanced Visual Assessment) SystemHEX · Traditional Mobileodt , Ltd.12/19/2016SE
K160341Colposcope SystemHEX · Traditional Xuzhou Kernel Medical Equipment Co., Ltd.09/14/2016SE
K160380LT-300 HDHEX · Traditional Lutech Industries, Inc.05/13/2016SE
K151878Video ColposcopeHEX · Traditional Edan Instruments, Inc.12/01/2015SE
K143119LT-300 Video ColposcopeHEX · Traditional Lutech Industries, Inc.12/18/2014SE

More from Lutech Industries, Inc.

510(k)DeviceDecision
K771898Automated Slide SpinnerGKJ · Traditional 10/18/1977SE
K771815SigmoscopeFAM · Traditional 10/07/1977SE
K770896Colposcope Model IIHEX · Traditional 06/03/1977SE
K770614Monitor, Gas ManifoldBXH · Traditional 04/07/1977SE
K760763Colposcope (Dynatech Colposcope-Model IHEX · Traditional 10/20/1976SE

Questions and answers

When was Dynatech JD7/JD7P Colposcope cleared by the FDA?

Dynatech JD7/JD7P Colposcope (K761205) received a 510(k) decision of Substantially Equivalent on December 17, 1976, 10 days after the submission was received.

What is the product code of K761205?

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