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FDA 510(k)

PULSE GENERATOR, CYBERLITH IMPLANTABLE

K-Number: K790221 · 1979-01-30

ApplicantIntermedics, Inc.
Decision Date1979-01-30
Product Code
DecisionUnknown

Device Summary

PULSE GENERATOR, CYBERLITH IMPLANTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1979-01-30 under 510(k) number K790221. FDA Decision: Unknown.

Frequently Asked Questions

What is the PULSE GENERATOR, CYBERLITH IMPLANTABLE?

PULSE GENERATOR, CYBERLITH IMPLANTABLE is a medical device that received FDA 510(k) clearance on 1979-01-30. The listed applicant is Intermedics, Inc.. The 510(k) number is K790221.

When did PULSE GENERATOR, CYBERLITH IMPLANTABLE receive FDA 510(k) clearance?

PULSE GENERATOR, CYBERLITH IMPLANTABLE received FDA 510(k) clearance on 1979-01-30, under 510(k) number K790221.

Who is the listed applicant for PULSE GENERATOR, CYBERLITH IMPLANTABLE?

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

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Other records listing Intermedics, 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.

K954610MODEL 430-07 ENDOCARDIAL PACING LEADK955122INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEADK962174BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)K955550CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEADK960281IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORYK954719INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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