ELECTROSURGICAL HEMOSTATIC FORCEPS SERIES— 510(k) K062517
Substantially EquivalentOlympus Medical Systems Corporation
FDA 510(k) clearance K062517 for ELECTROSURGICAL HEMOSTATIC FORCEPS SERIES, Substantially Equivalent on 2006-12-22. Applicant: Olympus Medical Systems Corporation. Device class: 2.
Clearance details
- Applicant
- Olympus Medical Systems Corporation
- Product code
- Code KGE
- Device class
- Class 2
- Regulation
- 21 CFR 876.4300
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Center Valley, PA, US
Recent devices under product code KGE
view all- K251807 — Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR
- K250187 — Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)
- K242857 — ClearHemograsper
- K231721 — Disposable Hot Biopsy Forceps
- K220053 — Diathermic Slitter (FlushKnife) DK2620JI and DK2623JI
More clearances from Olympus Medical Systems Corporation
view all- K260401 — EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE OLYMPUS BF-UCP190F (BF-UCP190F)
- K260824 — Gastrointestinal Videoscope Olympus GIF-2T1500
- K260856 — Disposable Distal Attachment D-201-13404
- K261183 — EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)
- K261260 — HD Camera Head OLYMPUS CH-S200-08-LB
Data sourced from openFDA. This site is unofficial and independent of the FDA.