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FDA 510(k)

PERIMETER THORACIC CATHETER

K-Number: K844922 · 1985-03-18

ApplicantPerimeter Medical, Inc.
Decision Date1985-03-18
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERIMETER THORACIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Perimeter Medical, Inc.. It received FDA 510(k) clearance on 1985-03-18 under 510(k) number K844922. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIMETER THORACIC CATHETER?

PERIMETER THORACIC CATHETER is a medical device that received FDA 510(k) clearance on 1985-03-18. The listed applicant is Perimeter Medical, Inc.. The 510(k) number is K844922.

When did PERIMETER THORACIC CATHETER receive FDA 510(k) clearance?

PERIMETER THORACIC CATHETER received FDA 510(k) clearance on 1985-03-18, under 510(k) number K844922.

Who is the listed applicant for PERIMETER THORACIC CATHETER?

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

What is the FDA product code for PERIMETER THORACIC CATHETER?

The FDA product code for PERIMETER THORACIC CATHETER is GBX.

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 Perimeter 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.

K844921PERIMETER CLOSED WOUND RESEVOIRK844924PERIMETER YANKAUER SUCTION TIPS & SETSK844925PERIMETER MEDIASTINAL DRAINK844923PERIMETER SUMP DRAIN

Related Devices (Code: GBX)

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.

K082725GRAFTGUARD PRESSURE CONTROLLING SYRINGEMaquet Cardiovascular, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, Inc.

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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