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FDA 510(k)

PACING KIT, SEMI-FLOATING

K-Number: K770018 · 1977-01-14

ApplicantElectro-Catheter Corp.
Decision Date1977-01-14
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PACING KIT, SEMI-FLOATING is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Catheter Corp.. It received FDA 510(k) clearance on 1977-01-14 under 510(k) number K770018. The device is classified under product code DTR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACING KIT, SEMI-FLOATING?

PACING KIT, SEMI-FLOATING is a medical device that received FDA 510(k) clearance on 1977-01-14. The listed applicant is Electro-Catheter Corp.. The 510(k) number is K770018.

When did PACING KIT, SEMI-FLOATING receive FDA 510(k) clearance?

PACING KIT, SEMI-FLOATING received FDA 510(k) clearance on 1977-01-14, under 510(k) number K770018.

Who is the listed applicant for PACING KIT, SEMI-FLOATING?

The FDA 510(k) record lists Electro-Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PACING KIT, SEMI-FLOATING?

The FDA product code for PACING KIT, SEMI-FLOATING is DTR.

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Other records listing Electro-Catheter Corp. as applicant

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Related Devices (Code: DTR)

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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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