MAGILL CATHETER INTRO. FORCEPS— 510(k) K801273
Substantially EquivalentJ. Sklar Mfg. Co., Inc.
FDA 510(k) clearance K801273 for MAGILL CATHETER INTRO. FORCEPS, Substantially Equivalent on 1980-07-28. Applicant: J. Sklar Mfg. Co., Inc.. Device class: 1.
Clearance details
- Applicant
- J. Sklar Mfg. Co., Inc.
- Product code
- Code KOA
- Device class
- Class 1
- Regulation
- 21 CFR 876.4730
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code KOA
view allMore clearances from J. Sklar Mfg. Co., Inc.
view allRecalls naming K801273
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 K801273.
Data sourced from openFDA. This site is unofficial and independent of the FDA.