FDA 510(k)

CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK.

K-Number: K874158 · 1987-12-29

Decision Date1987-12-29

Product CodeDXY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK. 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 1987-12-29 under 510(k) number K874158. 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.

Frequently Asked Questions

What is the CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK.?

CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK. is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Cardiac Control Systems, Inc.. The 510(k) number is K874158.

When did CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK. receive FDA 510(k) clearance?

CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK. received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874158.

Who is the listed applicant for CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK.?

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 CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK.?

The FDA product code for CCS IMPLANTABLE MAESTRO(R) SERIES 100/200 PACEMAK. is DXY. This falls under the Clinical Chemistry category.

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Other records listing Cardiac Control Systems, Inc. as applicant

K971775INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610 K946188CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER 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

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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.