FDA 510(k)

OsteoProbe

K-Number: K221195 · 2022-06-28

Decision Date2022-06-28

Product CodeQGQ

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

OsteoProbe is the device name listed in this FDA 510(k) record. The listed applicant is Active Life Scientific, Inc.. It received FDA 510(k) clearance on 2022-06-28 under 510(k) 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. The listed applicant is Active Life Scientific, Inc.. The 510(k) number is K221195.

When did OsteoProbe receive FDA 510(k) clearance?

OsteoProbe received FDA 510(k) clearance on 2022-06-28, under 510(k) number K221195.

Who is the listed applicant for OsteoProbe?

The FDA 510(k) record lists Active Life Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OsteoProbe?

The FDA product code for OsteoProbe is QGQ.

Other records listing Active Life Scientific, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250216OsteoProbe (OP-100)

Related Devices (Code: QGQ)

K250216OsteoProbe (OP-100)Active Life Scientific, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.