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FDA 510(k)

MINIATURIZE CHEST COMPRESSOR (MCC)

K-Number: K102068 · 2010-11-16

ApplicantResuscitation International
Decision Date2010-11-16
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIATURIZE CHEST COMPRESSOR (MCC) is the device name listed in this FDA 510(k) record. The listed applicant is Resuscitation International. It received FDA 510(k) clearance on 2010-11-16 under 510(k) number K102068. 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 MINIATURIZE CHEST COMPRESSOR (MCC)?

MINIATURIZE CHEST COMPRESSOR (MCC) is a medical device that received FDA 510(k) clearance on 2010-11-16. The listed applicant is Resuscitation International. The 510(k) number is K102068.

When did MINIATURIZE CHEST COMPRESSOR (MCC) receive FDA 510(k) clearance?

MINIATURIZE CHEST COMPRESSOR (MCC) received FDA 510(k) clearance on 2010-11-16, under 510(k) number K102068.

Who is the listed applicant for MINIATURIZE CHEST COMPRESSOR (MCC)?

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

What is the FDA product code for MINIATURIZE CHEST COMPRESSOR (MCC)?

The FDA product code for MINIATURIZE CHEST COMPRESSOR (MCC) 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

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

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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