CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS— 510(k) K946109
Substantially EquivalentCabot Medical Corp.
FDA 510(k) clearance K946109 for CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS, Substantially Equivalent on 1995-11-21. Applicant: Cabot Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Cabot Medical Corp.
- Product code
- Code KNS
- Device class
- Class 2
- Regulation
- 21 CFR 876.4300
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Langhorne, PA, US
Recent devices under product code KNS
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view all- K960148 — CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT
- 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
- K934115 — 3000 ELECTRONIC INSUFFLATOR MODIFICATION
Adverse events under product code KNS
product code KNS- Death
- 44
- Injury
- 2,361
- Malfunction
- 4,771
- Total
- 7,176
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.