Hysterscope
FDA 510(k) K940316 · Stephen Chakoff, Inc.
510(k) numberK940316
Submission
- Device name
- Hysterscope
- Applicant
- Stephen Chakoff, Inc.
Miami, FL, US - Received
- January 24, 1994
- Decision date
- November 16, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- HIH – Hysteroscope (And Accessories)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.1690
- Specialty
- Obstetrics/Gynecology
Other 510(k)s with product code HIH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254294 | Single-use Digital Hysteroscope (GYUT-A 12.6- 0, GYUT-A12.6- 12, GYUT-A 12.6- 22, GYUT-A…HIH · Traditional | Zhejiang Geyi Medical Instrument Co., Ltd. | 09/08/2026SE |
| K260984 | HERizon RD5 Resecting Device (5FR1PK);HERizon RD5 Resecting Device - 5 pack (5FR5PK)HIH · Traditional | Axora Medical, Inc. | 08/18/2026SE |
| K253020 | Strauss Surgical Resection InstrumentsHIH · Traditional | American Medical Endoscopy, Inc. | 06/04/2026SE |
| K254050 | Manual Tissue Removal DeviceHIH · Traditional | Suzhou AcuVu Medical Technology Co., Ltd. | 05/15/2026SE |
| K254251 | InnovexView (GC146-17, GC150-20, GC155-23)HIH · Traditional | Shanghai AnQing Medical Instrument Co., Ltd. | 02/26/2026SE |
| K252793 | ARMI® Endoscopic Video Image Processor (JY-MIP-3000); ARMI® Single-Use Hysteroscope…HIH · Traditional | Jiangsu Jiyuan Medical Technology Co., Ltd. | 12/18/2025SE |
| K252012 | SPY Cystoscope/HysteroscopeHIH · Special | Stryker Endoscopy | 07/18/2025SE |
| K243382 | RZ Resectoscope SystemHIH · Traditional | Rz Medizintechnik GmbH | 06/03/2025SE |
| K240978 | SeleneView® Single-Use Digital Hysteroscope (HC29, HC29-G, HC35, HC35-G, HO35, HO35-G…HIH · Traditional | MacroLux Medical Technology Co., Ltd. | 08/16/2024SE |
| K241987 | Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)HIH · Special | Guangzhou Red Pine Medical Instrument Co., Ltd. | 08/02/2024SE |
More from Guangzhou Red Pine Medical Instrument Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K940317 | SinuscopeEOB · Traditional | 05/24/1995SE |
| K950753 | Chakoff Endoscopy (Camera Television Endoscopic Without AudioGCJ · Traditional | 05/15/1995SE |
| K951082 | Chakoff Endoscopy, Rigid EndoscopeGCJ · Traditional | 03/22/1995SE |
| K950748 | Chakoff Endoscopy (Fiber Optic Light Source Routine)GCJ · Traditional | 03/06/1995SE |
| K950747 | Chakoff Endoscopy (Light Source Endoscopic Xenon Arc.)GCJ · Traditional | 03/06/1995SE |
| K950746 | Chakoff Endoscopy (Set Laparoscopy)GCJ · Traditional | 03/06/1995SE |
| K950745 | Chakoff Endoscopy (Endoscope And/Or Accessories)GCJ · Traditional | 03/06/1995SE |
| K950744 | Chakoff Endoscopy (Ridgid Endoscope)GCJ · Traditional | 03/06/1995SE |
| K945421 | Chakoff EndoscopyFDG · Traditional | 12/23/1994SE |
| K945420 | Chakoff EndoscopyFCW · Traditional | 12/08/1994SE |
Questions and answers
When was Hysterscope cleared by the FDA?
Hysterscope (K940316) received a 510(k) decision of Substantially Equivalent on November 16, 1995, 661 days after the submission was received.
What is the product code of K940316?
The FDA product code is HIH – Hysteroscope (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1690.