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FDA 510(k)

ATI MEDICAL COMFORT PLUS CPM PAD

K-Number: K910026 · 1991-01-18

ApplicantAti Medical, Inc.
Decision Date1991-01-18
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ATI MEDICAL COMFORT PLUS CPM PAD is the device name listed in this FDA 510(k) record. The listed applicant is Ati Medical, Inc.. It received FDA 510(k) clearance on 1991-01-18 under 510(k) number K910026. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATI MEDICAL COMFORT PLUS CPM PAD?

ATI MEDICAL COMFORT PLUS CPM PAD is a medical device that received FDA 510(k) clearance on 1991-01-18. The listed applicant is Ati Medical, Inc.. The 510(k) number is K910026.

When did ATI MEDICAL COMFORT PLUS CPM PAD receive FDA 510(k) clearance?

ATI MEDICAL COMFORT PLUS CPM PAD received FDA 510(k) clearance on 1991-01-18, under 510(k) number K910026.

Who is the listed applicant for ATI MEDICAL COMFORT PLUS CPM PAD?

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

What is the FDA product code for ATI MEDICAL COMFORT PLUS CPM PAD?

The FDA product code for ATI MEDICAL COMFORT PLUS CPM PAD is BXB.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ati Medical, 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.

K020683ISOROD PD-103 IMPLANT, MODEL ATI-PD-103

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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.

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