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Accelerated Care Plus Corp.

FDA Regulatory Profile

Accelerated Care Plus Corp. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 14, 2016.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K153456Megapulse III Shortwave DiathermyJune 14, 2016
K093600OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEMDecember 4, 2009
K060191ACP OMNIPAD LIGHT THERAPY SYSTEM & ACP OMNIPAD 500 CONTROL UNITJuly 12, 2006

FDA data resources