510(k) K831226
K831226 is an FDA 510(k) premarket notification submitted by Ballard Medical Products for the device "MEDICAL PRODUCTS FOAM DOUBLE SCRUB #450". The FDA issued a decision of Substantially Equivalent on May 16, 1983. The device falls under product code GEC (Brush, Scrub, Operating-Room), a Class I device regulated under 21 CFR 878.4800. Ballard Medical Products has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 16, 1983
- Date Received
- April 15, 1983
- 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