510(k) K831226

MEDICAL PRODUCTS FOAM DOUBLE SCRUB #450 by Ballard Medical Products — Product Code GEC

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