510(k) K241523
K241523 is an FDA 510(k) premarket notification submitted by Laborie Medical Technologies, Corp. for the device "injeTAK Adjustable Tip Needle (DIS199; DIS201)". The FDA issued a decision of Substantially Equivalent on August 27, 2024. The device falls under product code FBK (Endoscopic Injection Needle, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Laborie Medical Technologies, Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 27, 2024
- Date Received
- May 29, 2024
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscopic Injection Needle, Gastroenterology-Urology
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.