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FDA 510(k)

MODELS 5976/5977 PACEMAKER PULSE GENER

K-Number: K810677 · 1981-05-27

ApplicantMedtronic, Inc.
Decision Date1981-05-27
Product CodeDXY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS 5976/5977 PACEMAKER PULSE GENER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 1981-05-27 under 510(k) number K810677. 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 MODELS 5976/5977 PACEMAKER PULSE GENER?

MODELS 5976/5977 PACEMAKER PULSE GENER is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is Medtronic, Inc.. The 510(k) number is K810677.

When did MODELS 5976/5977 PACEMAKER PULSE GENER receive FDA 510(k) clearance?

MODELS 5976/5977 PACEMAKER PULSE GENER received FDA 510(k) clearance on 1981-05-27, under 510(k) number K810677.

Who is the listed applicant for MODELS 5976/5977 PACEMAKER PULSE GENER?

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

What is the FDA product code for MODELS 5976/5977 PACEMAKER PULSE GENER?

The FDA product code for MODELS 5976/5977 PACEMAKER PULSE GENER is DXY. This falls under the Clinical Chemistry category.

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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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