HM-0660
FDA 510(k) K932782 · Hill-Med, Inc.
510(k) numberK932782
Submission
- Device name
- HM-0660
- Applicant
- Hill-Med, Inc.
Miami, FL, US - Received
- June 9, 1993
- Decision date
- March 23, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement 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
Other 510(k)s with product code HEX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K233043 | Smart Scope® CXHEX · Traditional | Periwinkle Technologies Pvt., Ltd. | 06/14/2024SE |
| K190187 | Gynescope SystemHEX · Traditional | Illumigyn , Ltd. | 05/08/2019SE |
| K182764 | Biop Digital ColposcopeHEX · Traditional | Biop Medical , Ltd. | 11/27/2018SE |
| K181034 | Pocket Colposcope SystemHEX · Traditional | Hadleigh Health Technologies, LLC | 09/21/2018SE |
| K170446 | LT-300 SD Digital Video ColposcopeHEX · Traditional | Lutech Industries, Inc. | 05/21/2017SE |
| 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 |
More from Lutech Industries, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K993991 | HM-930 Electrosurgical UnitGEI · Traditional | 05/30/2000SE |
| K981781 | Electrosurgical UnitGEI · Traditional | 12/04/1998SE |
| K961473 | HM-88011 Solid State Electr Surgical UnitGEI · Traditional | 05/07/1996SE |
| K951718 | Hm-SpiroBZG · Traditional | 12/20/1995SE |
| K940140 | Hm-CryoGEH · Traditional | 06/27/1994SE |
| K932896 | HM-0690 ColposcopeHEX · Traditional | 03/23/1994SE |
| K932817 | HM-880 IGEI · Traditional | 03/09/1994SE |
| K932818 | HM-880GEI · Traditional | 02/25/1994SE |
| K932720 | HM-0970HRM · Traditional | 09/07/1993SE |
Questions and answers
When was HM-0660 cleared by the FDA?
HM-0660 (K932782) received a 510(k) decision of Substantially Equivalent on March 23, 1994, 287 days after the submission was received.
What is the product code of K932782?
The FDA product code is HEX – Colposcope (And Colpomicroscope), a Class II (moderate risk) device regulated under 21 CFR 884.1630.