SWEMED FOLLICLE ASPIRATION SET, DOUBLE LUMEN, SINGLE LUMEN, AND LUER NEEDLE— 510(k) K991273
Substantially EquivalentSwemed Lab International AB
FDA 510(k) clearance K991273 for SWEMED FOLLICLE ASPIRATION SET, DOUBLE LUMEN, SINGLE LUMEN, AND LUER NEEDLE, Substantially Equivalent on 1999-08-18. Applicant: Swemed Lab International AB. Device class: 2.
Clearance details
- Applicant
- Swemed Lab International AB
- Product code
- Code MQE
- Device class
- Class 2
- Regulation
- 21 CFR 884.6100
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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- K191291 — Wallace Dual Lumen Oocyte Recovery System
More clearances from Swemed Lab International AB
view all- K053208 — CLEAR VISION EMBRYO TRANSFER CATHETER SET, MODEL B100000 - B 100007; CLEAR VISION TRIAL TRANSFER CATHETER SET
- K022643 — BLASTOMERE BIOPSY PIPETTE, MODELS H-55530 AND H-55540
- K991700 — SWEMED INTRACYTOPLASMIC SPERM INJECTION (ICSI) MICRO-INJECTION PIPETTES; HOLDING PIPTTES; DENUDING PIPETTES; ASSISTED/ZO
Data sourced from openFDA. This site is unofficial and independent of the FDA.