FDA 510(k)

MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER

K-Number: K880422 · 1988-03-31

Decision Date1988-03-31

Product CodeDXY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MAESTRO(R) MODEL 119, SINGLE-CHAMBER 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 1988-03-31 under 510(k) number K880422. 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 MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER?

MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Cardiac Control Systems, Inc.. The 510(k) number is K880422.

When did MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER receive FDA 510(k) clearance?

MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880422.

Who is the listed applicant for MAESTRO(R) MODEL 119, SINGLE-CHAMBER 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 MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER?

The FDA product code for MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER is DXY. This falls under the Clinical Chemistry category.

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Other records listing Cardiac Control Systems, Inc. as applicant

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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.