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FDA 510(k)

STAT-PAD (TM)

K-Number: K871538 · 1987-06-24

ApplicantCardiac Resucitator Corp.
Decision Date1987-06-24
Product CodeDRO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STAT-PAD (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Resucitator Corp.. It received FDA 510(k) clearance on 1987-06-24 under 510(k) number K871538. The device is classified under product code DRO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAT-PAD (TM)?

STAT-PAD (TM) is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Cardiac Resucitator Corp.. The 510(k) number is K871538.

When did STAT-PAD (TM) receive FDA 510(k) clearance?

STAT-PAD (TM) received FDA 510(k) clearance on 1987-06-24, under 510(k) number K871538.

Who is the listed applicant for STAT-PAD (TM)?

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

What is the FDA product code for STAT-PAD (TM)?

The FDA product code for STAT-PAD (TM) is DRO.

Other records listing Cardiac Resucitator 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.

K882513MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORK871971MODIFIED PACE*AID MODEL 53K871569MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORK870622HEART*AID 1000K850596PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &K850170HEART AID MODEL 97

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Related Devices (Code: DRO)

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.

K012218LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODESThe Ludlow Company LPK012404K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85Katecho, Inc.K000660ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413Medical Data ElectronicsK983196PADTAK PACE/DEFIB/CARDIOVERT MONITORING ELECTRODE(S)Tz Medical, Inc.K983232PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERTTz Medical, Inc.K974034PORTABLE INTENSIVE CARE UNITMedical Research Laboratories, 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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