ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT— 510(k) K093075
Substantially EquivalentAragon Surgical, Inc.
FDA 510(k) clearance K093075 for ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT, Substantially Equivalent on 2010-01-21. Applicant: Aragon Surgical, Inc.. Device class: 2.
Clearance details
- Applicant
- Aragon Surgical, Inc.
- Product code
- Code GEI
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
Recent devices under product code GEI
view allMore clearances from Aragon Surgical, Inc.
view allAdverse events under product code GEI
product code GEI- Death
- 133
- Injury
- 7,585
- Malfunction
- 35,808
- Other
- 44
- Total
- 43,570
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 →
Recalls naming K093075
K-number listed on FDA's recall record- Z-2496-2019 — CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
- Z-2497-2019 — CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM REF: PL731SU- Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K093075.
Data sourced from openFDA. This site is unofficial and independent of the FDA.