DeviceClearance

WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)— 510(k) K111392

Substantially Equivalent

Woojeon Company

FDA 510(k) clearance K111392 for WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE), Substantially Equivalent on 2011-11-04. Applicant: Woojeon Company.

Clearance details

Applicant
Woojeon Company
Product code
Code MQX
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Pittsburgh, PA, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.