SUTURE REMOVAL KIT— 510(k) K761193
Substantially EquivalentSuperior Plastic Products Corp.
FDA 510(k) clearance K761193 for SUTURE REMOVAL KIT, Substantially Equivalent on 1977-01-12. Applicant: Superior Plastic Products Corp.. Device class: 1.
Clearance details
- Applicant
- Superior Plastic Products Corp.
- Product code
- Code KDD
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Superior Plastic Products Corp.
view allRecalls naming K761193
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 K761193.
Data sourced from openFDA. This site is unofficial and independent of the FDA.