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FDA 510(k)

ELGILOY STYLET

K-Number: K770243 · 1977-02-14

ApplicantCardiac Pacemakers, Inc.
Decision Date1977-02-14
Product CodeDRR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELGILOY STYLET is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Pacemakers, Inc.. It received FDA 510(k) clearance on 1977-02-14 under 510(k) number K770243. The device is classified under product code DRR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELGILOY STYLET?

ELGILOY STYLET is a medical device that received FDA 510(k) clearance on 1977-02-14. The listed applicant is Cardiac Pacemakers, Inc.. The 510(k) number is K770243.

When did ELGILOY STYLET receive FDA 510(k) clearance?

ELGILOY STYLET received FDA 510(k) clearance on 1977-02-14, under 510(k) number K770243.

Who is the listed applicant for ELGILOY STYLET?

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 ELGILOY STYLET?

The FDA product code for ELGILOY STYLET is DRR.

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Other records listing Cardiac Pacemakers, Inc. as applicant

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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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