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FDA 510(k)

ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER

K-Number: K002603 · 2001-01-08

ApplicantZcv ,Inc.
Decision Date2001-01-08
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Zcv ,Inc.. It received FDA 510(k) clearance on 2001-01-08 under 510(k) number K002603. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER?

ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER is a medical device that received FDA 510(k) clearance on 2001-01-08. The listed applicant is Zcv ,Inc.. The 510(k) number is K002603.

When did ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER receive FDA 510(k) clearance?

ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER received FDA 510(k) clearance on 2001-01-08, under 510(k) number K002603.

Who is the listed applicant for ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER?

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

What is the FDA product code for ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER?

The FDA product code for ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER is LDF.

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 Zcv ,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: LDF)

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

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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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