510(k) K854232
K854232 is an FDA 510(k) premarket notification submitted by American Pharmaseal Div. Ahsc for the device "PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES". The FDA issued a decision of SN on December 10, 1985. The device falls under product code GEC (Brush, Scrub, Operating-Room), a Class I device regulated under 21 CFR 878.4800. American Pharmaseal Div. Ahsc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- December 10, 1985
- Date Received
- October 21, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Brush, Scrub, Operating-Room
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type