PACEMAKER PROGRAMMER 2030
K-Number: K820230 · 1982-03-15
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Device Summary
Frequently Asked Questions
What is the PACEMAKER PROGRAMMER 2030?
PACEMAKER PROGRAMMER 2030 is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is Cardiac Pacemakers, Inc.. The 510(k) number is K820230.
When did PACEMAKER PROGRAMMER 2030 receive FDA 510(k) clearance?
PACEMAKER PROGRAMMER 2030 received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820230.
Who is the listed applicant for PACEMAKER PROGRAMMER 2030?
The FDA 510(k) record lists Cardiac Pacemakers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PACEMAKER PROGRAMMER 2030?
The FDA product code for PACEMAKER PROGRAMMER 2030 is KRG.
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.
Other records listing Cardiac Pacemakers, Inc. 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.
Related Devices (Code: KRG)
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.
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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