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FDA 510(k)

L-15T ENDOCARDIAL PACING ELECTRODE

K-Number: K802689 · 1980-10-28

ApplicantCoratomic, Inc.
Decision Date1980-10-28
Product Code
DecisionUnknown

Device Summary

L-15T ENDOCARDIAL PACING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Coratomic, Inc.. It received FDA 510(k) clearance on 1980-10-28 under 510(k) number K802689. FDA Decision: Unknown.

Frequently Asked Questions

What is the L-15T ENDOCARDIAL PACING ELECTRODE?

L-15T ENDOCARDIAL PACING ELECTRODE is a medical device that received FDA 510(k) clearance on 1980-10-28. The listed applicant is Coratomic, Inc.. The 510(k) number is K802689.

When did L-15T ENDOCARDIAL PACING ELECTRODE receive FDA 510(k) clearance?

L-15T ENDOCARDIAL PACING ELECTRODE received FDA 510(k) clearance on 1980-10-28, under 510(k) number K802689.

Who is the listed applicant for L-15T ENDOCARDIAL PACING ELECTRODE?

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

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Other records listing Coratomic, 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.

K863365MODIFICATION OF STERILITY CYCLE PARAMETERSK822791CORATOMIC #VX5-105 & VX5-205 PULSE GEN.K820939C-101-PK821014CORATOMIC MODEL OVALITH 920BPK821033CORATOMIC MODEL OVALITH-920K810808CORATOMIC MODEL OVALITH-920

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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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