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FDA 510(k)

CPR TRAVELER

K-Number: K801947 · 1980-11-19

ApplicantCardia Concepts Corp.
Decision Date1980-11-19
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPR TRAVELER is the device name listed in this FDA 510(k) record. The listed applicant is Cardia Concepts Corp.. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K801947. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR TRAVELER?

CPR TRAVELER is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Cardia Concepts Corp.. The 510(k) number is K801947.

When did CPR TRAVELER receive FDA 510(k) clearance?

CPR TRAVELER received FDA 510(k) clearance on 1980-11-19, under 510(k) number K801947.

Who is the listed applicant for CPR TRAVELER?

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

What is the FDA product code for CPR TRAVELER?

The FDA product code for CPR TRAVELER is DRM.

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 Cardia Concepts Corp. 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.

K801946CPR HELPERK801945SAVE MOR

Related Devices (Code: DRM)

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.

K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLCK173553LUCAS 3 Chest Compression SystemJolife ABK161768LUCAS 3 Chest Compression SystemJolife ABK153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLCK112998AUTOPULSE RESUSCITATION SYSTEM MODEL 1000Zoll Circulation

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.

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