ETHICON ENDO SURGERY SLOTTED ANOSCOPE— 510(k) K093896
Substantially EquivalentEthicon Endo-Surgery, Inc.
FDA 510(k) clearance K093896 for ETHICON ENDO SURGERY SLOTTED ANOSCOPE, Substantially Equivalent on 2010-03-25. Applicant: Ethicon Endo-Surgery, Inc.. Device class: 2.
Clearance details
- Applicant
- Ethicon Endo-Surgery, Inc.
- Product code
- Code FER
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
Recent devices under product code FER
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- K101520 — ENSEAL TISSUE SEALING DEVICES MODEL: NSEAL514H-535H, NSEAL514RH-535RH
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Data sourced from openFDA. This site is unofficial and independent of the FDA.