510(k) K871198
K871198 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "BONE MARROW COLLECTION KIT AND STAND". The FDA issued a decision of Substantially Equivalent on November 6, 1987. The device falls under product code LWE (Bone Marrow Collection/Transfusion Kit), a Class II device. Baxter Healthcare Corp has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 6, 1987
- Date Received
- March 24, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bone Marrow Collection/Transfusion Kit
- Device Class
- Class II
- Regulation Number
- Review Panel
- HO
- Submission Type
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.fda.gov/cdrh/ode/convkit.html.This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.