510(k) K940025
K940025 is an FDA 510(k) premarket notification submitted by Manan Medical Products, Inc. for the device "MANAN BONE MARROW HARVEST NEEDLES". The FDA issued a decision of Substantially Equivalent on February 25, 1994. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Manan Medical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 25, 1994
- Date Received
- January 3, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Aspiration And Injection, Disposable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type