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FDA 510(k)

MAESTRO PACEMAKER TEST MAGNET

K-Number: K895110 · 1989-09-26

ApplicantCardiac Control Systems, Inc.
Decision Date1989-09-26
Product CodeDTG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAESTRO PACEMAKER TEST MAGNET is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Control Systems, Inc.. It received FDA 510(k) clearance on 1989-09-26 under 510(k) number K895110. 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 MAESTRO PACEMAKER TEST MAGNET?

MAESTRO PACEMAKER TEST MAGNET is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Cardiac Control Systems, Inc.. The 510(k) number is K895110.

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

MAESTRO PACEMAKER TEST MAGNET received FDA 510(k) clearance on 1989-09-26, under 510(k) number K895110.

Who is the listed applicant for MAESTRO PACEMAKER TEST MAGNET?

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

What is the FDA product code for MAESTRO PACEMAKER TEST MAGNET?

The FDA product code for MAESTRO PACEMAKER TEST MAGNET is DTG.

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 Cardiac Control Systems, Inc. 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.

K971775INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610K946188CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKERK950210CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKERK923868CCS MAESTRO II SERIES 200 CARDIAC PACEMAKERK905824MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKEK904941MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACE

View all 26 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.K831926IMPLANTABLE ENDOCARDIAL PACING LEADSOscor, Inc.K813153TEST MAGNETPacesetter Systems

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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