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FDA 510(k)

MODEL EC4542G MINIATURE

K-Number: K896352 · 1990-01-24

ApplicantPace Medical
Decision Date1990-01-24
Product CodeDTE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL EC4542G MINIATURE is the device name listed in this FDA 510(k) record. The listed applicant is Pace Medical. It received FDA 510(k) clearance on 1990-01-24 under 510(k) number K896352. 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 MODEL EC4542G MINIATURE?

MODEL EC4542G MINIATURE is a medical device that received FDA 510(k) clearance on 1990-01-24. The listed applicant is Pace Medical. The 510(k) number is K896352.

When did MODEL EC4542G MINIATURE receive FDA 510(k) clearance?

MODEL EC4542G MINIATURE received FDA 510(k) clearance on 1990-01-24, under 510(k) number K896352.

Who is the listed applicant for MODEL EC4542G MINIATURE?

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

What is the FDA product code for MODEL EC4542G MINIATURE?

The FDA product code for MODEL EC4542G MINIATURE is DTE.

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Other records listing Pace Medical 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.

K011980ADAPTER, PACING ANALYZER/UNIVERSAL PACING ADAPTER, MODELS 4820 AND 4825K012392DISPOSABLE SURGICAL EXTENSION CABLE, MODEL 4255 AND MODEL 4260K002204PACEMAKER EXTENSION CABLE MODELS 4265,4265A, 4265V, 5265, 5265A, 5265VK002497MODEL 4810 ANALYZER OUTPUT ADAPTERK002496MODEL 4815 ADAPTERK001180TEMPORARY PACEMAKER EXTENSION CABLE, MODELS 5235, 5235A, 5235V, TEMPORARY PACEMAKER SURGICAL EXTENSION CABLE, MODELS 528

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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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