510(k) K945109
K945109 is an FDA 510(k) premarket notification submitted by Sherwood Medical Co. for the device "MONOJECT BONE MARROW BIOPSY TRAYS". The FDA issued a decision of Substantially Equivalent on November 14, 1994. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Sherwood Medical Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 14, 1994
- Date Received
- October 18, 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