FDA 510(k)

CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER

K-Number: K946188 · 1995-05-15

Decision Date1995-05-15

Product CodeDXY

Advisory CommitteeCV

DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER 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 1995-05-15 under 510(k) number K946188. The device is classified under product code DXY. It was reviewed by the CV advisory panel. Product code DXY falls under the category of Clinical Chemistry, which covers reagents and instruments for chemical analysis of clinical samples. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER?

CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Cardiac Control Systems, Inc.. The 510(k) number is K946188.

When did CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER receive FDA 510(k) clearance?

CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER received FDA 510(k) clearance on 1995-05-15, under 510(k) number K946188.

Who is the listed applicant for CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER?

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 CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER?

The FDA product code for CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER is DXY. This falls under the Clinical Chemistry category.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cardiac Control Systems, Inc. as applicant

K971775INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610 K950210CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER K923868CCS MAESTRO II SERIES 200 CARDIAC PACEMAKER K905824MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE K904941MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACE K895110MAESTRO PACEMAKER TEST MAGNET

View all 26 devices →

Related Devices (Code: DXY)

K993434PIKOS 01, PIKOS E01, PIKOS 01-B, PIKOS E01-B, PIKOS 01-A, PIKOS E01-ABiotronik, Inc.K970072OPUS S MODEL 4121 AND 4124 PACEMAKERSEla Medical, Inc.K945627PIKOS LP 01, PIKOS LP E01Biotronik, Inc.K953866MINIX 834M & MINIX ST 8331M PULSE GENERATORS (MODIFICATION)Medtronic Vascular K954092ALTERNATE STERLIZATION PROCESS & MODIFIED DF-1 LEAD CONNECTOR (MODIFICATION)Medtronic Vascular K953417MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORSCook Pacemaker Corp.

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.