FDA 510(k)

deepLive

K-Number: K240610 · 2024-07-09

Decision Date2024-07-09

Product CodeNQQ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

deepLive is the device name listed in this FDA 510(k) record. The listed applicant is Damae Medical. It received FDA 510(k) clearance on 2024-07-09 under 510(k) number K240610. The device is classified under product code NQQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the deepLive?

deepLive is a medical device that received FDA 510(k) clearance on 2024-07-09. The listed applicant is Damae Medical. The 510(k) number is K240610.

When did deepLive receive FDA 510(k) clearance?

deepLive received FDA 510(k) clearance on 2024-07-09, under 510(k) number K240610.

Who is the listed applicant for deepLive?

The FDA 510(k) record lists Damae Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for deepLive?

The FDA product code for deepLive is NQQ.

Other records listing Damae Medical 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.

K252851deepLive (OSP12 + DMS)

Related Devices (Code: NQQ)

K253459OPTIS Mobile Next Imaging System (1014932); OPTIS Integrated Next Imaging System (1014933); Ultreon 3.0 Software Upgrade Kit (ULTR300001)ABBOTT MEDICAL K251730LIA Console (542-7)Leadoptik, Inc.K253101HyperVue™ Imaging System - IntegratedSpectrawave, Inc.K252851deepLive (OSP12 + DMS)Damae Medical K251198HyperVue™ SoftwareSpectrawave, Inc.K250684OPUSWAVE Dual Sensor Imaging SystemTerumo Cardiovascular Systems Thi Plant

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.