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FDA 510(k)

HASKEL CPR

K-Number: K922093 · 1994-03-14

ApplicantHaskel, Inc.
Decision Date1994-03-14
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HASKEL CPR is the device name listed in this FDA 510(k) record. The listed applicant is Haskel, Inc.. It received FDA 510(k) clearance on 1994-03-14 under 510(k) number K922093. 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 HASKEL CPR?

HASKEL CPR is a medical device that received FDA 510(k) clearance on 1994-03-14. The listed applicant is Haskel, Inc.. The 510(k) number is K922093.

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

HASKEL CPR received FDA 510(k) clearance on 1994-03-14, under 510(k) number K922093.

Who is the listed applicant for HASKEL CPR?

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

What is the FDA product code for HASKEL CPR?

The FDA product code for HASKEL CPR is DRM.

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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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