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FDA 510(k)

BRINDLEY & SMITH ET-1000

K-Number: K915100 · 1992-09-14

ApplicantZmi Corp.
Decision Date1992-09-14
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BRINDLEY & SMITH ET-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Zmi Corp.. It received FDA 510(k) clearance on 1992-09-14 under 510(k) number K915100. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRINDLEY & SMITH ET-1000?

BRINDLEY & SMITH ET-1000 is a medical device that received FDA 510(k) clearance on 1992-09-14. The listed applicant is Zmi Corp.. The 510(k) number is K915100.

When did BRINDLEY & SMITH ET-1000 receive FDA 510(k) clearance?

BRINDLEY & SMITH ET-1000 received FDA 510(k) clearance on 1992-09-14, under 510(k) number K915100.

Who is the listed applicant for BRINDLEY & SMITH ET-1000?

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

What is the FDA product code for BRINDLEY & SMITH ET-1000?

The FDA product code for BRINDLEY & SMITH ET-1000 is LIH.

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Other records listing Zmi 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.

K915159PEDIATRIC MULTI-FUNCTION ELECTRODESK913484ZOLL D-900 DEFIBRILLATORK911956ZOLL PD-1400 PACER/DEFIBRILLATORK895032ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODESK885166ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODESK873402ZOLL NTP-1200 PACER/DEFIBRILLATOR

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Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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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