Optus Hysteroscopes and Contact Hysteroscopes
FDA 510(k) K945265 · Optus, Inc.
510(k) numberK945265
Submission
- Device name
- Optus Hysteroscopes and Contact Hysteroscopes
- Applicant
- Optus, Inc.
Denver, CO, US - Received
- October 28, 1994
- Decision date
- September 12, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement 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 |
|---|---|---|
| K945264 | Optus OtoscopesERA · Traditional | 02/02/1996SE |
| K953913 | Optus Arthroscope & Mini-Arthroscope AccessoriesHRX · Traditional | 01/22/1996SE |
| K945268 | Optus BronchoscopesEOQ · Traditional | 12/21/1995SE |
| K945262 | Optus Cystoscopes and Pediatric CystoscopesFAJ · Traditional | 05/26/1995SE |
| K945267 | Optus Arthroscopes and Mini-ArthroscopesHRX · Traditional | 05/23/1995SE |
| K945266 | Optus Laparoscopes and Operating LaparoscopesGCJ · Traditional | 02/23/1995SE |
| K944656 | Optus Sinuscopes and AccessoriesEOB · Traditional | 01/26/1995SE |
| K945263 | Optus ThoracoscopesGCJ · Traditional | 12/13/1994SE |
| K945269 | Optus LaryngoscopesCCW · Traditional | 11/07/1994SE |
Questions and answers
When was Optus Hysteroscopes and Contact Hysteroscopes cleared by the FDA?
Optus Hysteroscopes and Contact Hysteroscopes (K945265) received a 510(k) decision of Substantially Equivalent on September 12, 1995, 319 days after the submission was received.
What is the product code of K945265?
The FDA product code is HIH – Hysteroscope (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1690.