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FDA 510(k)

THUMPER CARDIOPULMONARY RESUSCITATOR 1005

K-Number: K851139 · 1985-05-15

ApplicantMichigan Instruments, Inc.
Decision Date1985-05-15
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THUMPER CARDIOPULMONARY RESUSCITATOR 1005 is the device name listed in this FDA 510(k) record. The listed applicant is Michigan Instruments, Inc.. It received FDA 510(k) clearance on 1985-05-15 under 510(k) number K851139. 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 THUMPER CARDIOPULMONARY RESUSCITATOR 1005?

THUMPER CARDIOPULMONARY RESUSCITATOR 1005 is a medical device that received FDA 510(k) clearance on 1985-05-15. The listed applicant is Michigan Instruments, Inc.. The 510(k) number is K851139.

When did THUMPER CARDIOPULMONARY RESUSCITATOR 1005 receive FDA 510(k) clearance?

THUMPER CARDIOPULMONARY RESUSCITATOR 1005 received FDA 510(k) clearance on 1985-05-15, under 510(k) number K851139.

Who is the listed applicant for THUMPER CARDIOPULMONARY RESUSCITATOR 1005?

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

What is the FDA product code for THUMPER CARDIOPULMONARY RESUSCITATOR 1005?

The FDA product code for THUMPER CARDIOPULMONARY RESUSCITATOR 1005 is DRM.

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Other records listing Michigan Instruments, 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.

K073079THUMPER, MODEL: 1008K972525THUMPERK962237THUMPER CARDIOPULMONARY RESUSCITATORK895954LARYNGOSTAT LARYNGOSCOPE HANDLEK833879CARDIOPULMONARY RESUSCITATORK811909CARDIOPULMUNARY RESUSCITATOR

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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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