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FDA 510(k)

PROLITH MODEL 21S CARDIAC PULSE GEN.

K-Number: K770212 · 1977-03-09

ApplicantEdwards Pacemaker Systems
Decision Date1977-03-09
Product CodeDXY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROLITH MODEL 21S CARDIAC PULSE GEN. is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Pacemaker Systems. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770212. 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 PROLITH MODEL 21S CARDIAC PULSE GEN.?

PROLITH MODEL 21S CARDIAC PULSE GEN. is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Edwards Pacemaker Systems. The 510(k) number is K770212.

When did PROLITH MODEL 21S CARDIAC PULSE GEN. receive FDA 510(k) clearance?

PROLITH MODEL 21S CARDIAC PULSE GEN. received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770212.

Who is the listed applicant for PROLITH MODEL 21S CARDIAC PULSE GEN.?

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

What is the FDA product code for PROLITH MODEL 21S CARDIAC PULSE GEN.?

The FDA product code for PROLITH MODEL 21S CARDIAC PULSE GEN. 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.

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Other records listing Edwards Pacemaker 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.

K791751EDWARDS PACEMAKER 30 UNIPOLAR GENERATORK79045228 UNIPOLAR AND BIPOLAR PULSE GENERATORSK781111LEAD CONVERSION KIT, MODEL 341K781144ANALYZER, PACER SYSTEM, PSA-5K781042PROLITH 23S PACEMAKERK780780MICROPULSE 22S PACEMAKER

View all 13 devices →

Related Devices (Code: DXY)

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.

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 VascularK954092ALTERNATE STERLIZATION PROCESS & MODIFIED DF-1 LEAD CONNECTOR (MODIFICATION)Medtronic VascularK953417MINIFLEX 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.

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