SUNDASH— 510(k) K932483
Substantially EquivalentSun Ind., Inc.
FDA 510(k) clearance K932483 for SUNDASH, Substantially Equivalent on 1994-02-22. Applicant: Sun Ind., Inc.. Device class: 2.
Clearance details
- Applicant
- Sun Ind., Inc.
- Product code
- Code LEJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4635
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jonesboro, AR, US
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More clearances from Sun Ind., Inc.
view allRecalls naming K932483
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K932483.
Data sourced from openFDA. This site is unofficial and independent of the FDA.