ELECTRO-GYNE ELECTROSURGICAL GENERATOR— 510(k) K871960
Substantially EquivalentCabot Medical Corp.
FDA 510(k) clearance K871960 for ELECTRO-GYNE ELECTROSURGICAL GENERATOR, Substantially Equivalent on 1987-07-10. Applicant: Cabot Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Cabot Medical Corp.
- Product code
- Code KNF
- Device class
- Class 2
- Regulation
- 21 CFR 884.4160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Langhorne, PA, US
Recent devices under product code KNF
view all- K250705 — Sonata Transcervical Fibroid Ablation System 2.2
- K240503 — Sonata Transcervical Fibroid Ablation System 2.2
- K233848 — Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)
- K222304 — Sonata Transcervical Fibroid Ablation System 2.2
- K211535 — Sonata Transcervical Fibroid Ablation System 2.2
More clearances from Cabot Medical Corp.
view all- K960148 — CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT
- K946109 — CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS
- K951972 — CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHS
- K951714 — CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER
- K941743 — CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP
Data sourced from openFDA. This site is unofficial and independent of the FDA.