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FDA 510(k)

TEST MAGNET

K-Number: K813153 · 1981-12-02

ApplicantPacesetter Systems
Decision Date1981-12-02
Product CodeDTG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TEST MAGNET is the device name listed in this FDA 510(k) record. The listed applicant is Pacesetter Systems. It received FDA 510(k) clearance on 1981-12-02 under 510(k) number K813153. The device is classified under product code DTG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST MAGNET?

TEST MAGNET is a medical device that received FDA 510(k) clearance on 1981-12-02. The listed applicant is Pacesetter Systems. The 510(k) number is K813153.

When did TEST MAGNET receive FDA 510(k) clearance?

TEST MAGNET received FDA 510(k) clearance on 1981-12-02, under 510(k) number K813153.

Who is the listed applicant for TEST MAGNET?

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

What is the FDA product code for TEST MAGNET?

The FDA product code for TEST MAGNET is DTG.

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Other records listing Pacesetter Systems 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.

K910924ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONEK902147ENDOCARDIAL SCREW-IN LEAD MODEL 1028TK900512SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERSK900550FAST-PASS ACE MODELS 1212T/1222T/1216T/1226TK895447ENDOCARDIAL SCREW-IN LEAD MODEL 1020TK891905CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

View all 96 devices →

Related Devices (Code: DTG)

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.

K092364MODEL 220 PATIENT MAGNETCyberonics, Inc.K960849MAGNO ALARMCardiac Assist Devices, Inc.K895110MAESTRO PACEMAKER TEST MAGNETCardiac Control Systems, Inc.K831926IMPLANTABLE ENDOCARDIAL PACING LEADSOscor, 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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