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FDA 510(k)

SIEMENS MODEL 146-146A EXTERNAL PULSE G

K-Number: K810566 · 1981-04-01

ApplicantCynergy
Decision Date1981-04-01
Product CodeDTE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS MODEL 146-146A EXTERNAL PULSE G is the device name listed in this FDA 510(k) record. The listed applicant is Cynergy. It received FDA 510(k) clearance on 1981-04-01 under 510(k) number K810566. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MODEL 146-146A EXTERNAL PULSE G?

SIEMENS MODEL 146-146A EXTERNAL PULSE G is a medical device that received FDA 510(k) clearance on 1981-04-01. The listed applicant is Cynergy. The 510(k) number is K810566.

When did SIEMENS MODEL 146-146A EXTERNAL PULSE G receive FDA 510(k) clearance?

SIEMENS MODEL 146-146A EXTERNAL PULSE G received FDA 510(k) clearance on 1981-04-01, under 510(k) number K810566.

Who is the listed applicant for SIEMENS MODEL 146-146A EXTERNAL PULSE G?

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

What is the FDA product code for SIEMENS MODEL 146-146A EXTERNAL PULSE G?

The FDA product code for SIEMENS MODEL 146-146A EXTERNAL PULSE G is DTE.

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.

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Other records listing Cynergy 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.

K801596CYNERGY MODEL 184K792536CYNERGY MODEL 182K792223PACESETTER MODEL 350K781407ERM-101

Related Devices (Code: DTE)

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.

K241781Solo Pace ControlSolo Pace, Inc.K232721Lifetech Cardio Temporary PacemakerShenzhen Lifetech Cardio Medical Electronics Co., Ltd.K201011Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.K190825Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.K182839Lifetech Cardio Model 8301 Temporary PacemakerShenzhen Lifetech Cardio Medical Electronics Co., Ltd.K181973Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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