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FDA 510(k)

CYNERGY MODEL 182

K-Number: K792536 · 1980-01-31

ApplicantCynergy
Decision Date1980-01-31
Product CodeDTE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CYNERGY MODEL 182 is the device name listed in this FDA 510(k) record. The listed applicant is Cynergy. It received FDA 510(k) clearance on 1980-01-31 under 510(k) number K792536. 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 CYNERGY MODEL 182?

CYNERGY MODEL 182 is a medical device that received FDA 510(k) clearance on 1980-01-31. The listed applicant is Cynergy. The 510(k) number is K792536.

When did CYNERGY MODEL 182 receive FDA 510(k) clearance?

CYNERGY MODEL 182 received FDA 510(k) clearance on 1980-01-31, under 510(k) number K792536.

Who is the listed applicant for CYNERGY MODEL 182?

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 CYNERGY MODEL 182?

The FDA product code for CYNERGY MODEL 182 is DTE.

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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.

K810566SIEMENS MODEL 146-146A EXTERNAL PULSE GK801596CYNERGY MODEL 184K792223PACESETTER 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

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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