OsteoProbe
K-Number: K221195 · 2022-06-28
ApplicantActive Life Scientific, Inc.
Decision Date2022-06-28
Product CodeQGQ
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
OsteoProbe is a medical device manufactured by Active Life Scientific, Inc.. It received FDA 510(k) clearance on 2022-06-28 under approval number K221195. The device is classified under product code QGQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the OsteoProbe?
OsteoProbe is a medical device that received FDA 510(k) clearance on 2022-06-28. It is manufactured by Active Life Scientific, Inc.. The 510(k) number is K221195.
When was OsteoProbe approved by the FDA?
OsteoProbe received FDA 510(k) clearance on 2022-06-28, under approval number K221195.
What company makes OsteoProbe?
OsteoProbe is manufactured by Active Life Scientific, Inc..
What is the FDA product code for OsteoProbe?
The FDA product code for OsteoProbe is QGQ.
Other Devices by Active Life Scientific, Inc.
Related Devices (Code: QGQ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.