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FDA 510(k)

PXI PNEUMATIC COMPRESSION PADDLE

K-Number: K913436 · 1992-11-05

ApplicantBrotherston/Pxi
Decision Date1992-11-05
Product CodeIZG
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PXI PNEUMATIC COMPRESSION PADDLE is the device name listed in this FDA 510(k) record. The listed applicant is Brotherston/Pxi. It received FDA 510(k) clearance on 1992-11-05 under 510(k) number K913436. The device is classified under product code IZG. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PXI PNEUMATIC COMPRESSION PADDLE?

PXI PNEUMATIC COMPRESSION PADDLE is a medical device that received FDA 510(k) clearance on 1992-11-05. The listed applicant is Brotherston/Pxi. The 510(k) number is K913436.

When did PXI PNEUMATIC COMPRESSION PADDLE receive FDA 510(k) clearance?

PXI PNEUMATIC COMPRESSION PADDLE received FDA 510(k) clearance on 1992-11-05, under 510(k) number K913436.

Who is the listed applicant for PXI PNEUMATIC COMPRESSION PADDLE?

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

What is the FDA product code for PXI PNEUMATIC COMPRESSION PADDLE?

The FDA product code for PXI PNEUMATIC COMPRESSION PADDLE is IZG.

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 Brotherston/Pxi 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.

K913435PXI URCD

Related Devices (Code: IZG)

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.

K960082DISCOGRAPHY KITSpinal Specialties, Inc.K960146G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAYGE Medical SystemsK920393MU125M MOBILE X-RAY SYSTEMShimadzu Medical SystemsK910503DISCOGRAPHY KITB. Braun of America, Inc.K903808AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KITAdvanced Med/Surg, Inc.K892659ELECTRODELCAOldelft Corp. of America

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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