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FDA 510(k)

BALLOON TEMP. PACING CATHETER

K-Number: K822003 · 1982-10-15

Decision Date1982-10-15
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BALLOON TEMP. PACING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Ziehm International, Inc.. It received FDA 510(k) clearance on 1982-10-15 under 510(k) number K822003. 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 BALLOON TEMP. PACING CATHETER?

BALLOON TEMP. PACING CATHETER is a medical device that received FDA 510(k) clearance on 1982-10-15. The listed applicant is Ziehm International, Inc.. The 510(k) number is K822003.

When did BALLOON TEMP. PACING CATHETER receive FDA 510(k) clearance?

BALLOON TEMP. PACING CATHETER received FDA 510(k) clearance on 1982-10-15, under 510(k) number K822003.

Who is the listed applicant for BALLOON TEMP. PACING CATHETER?

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

What is the FDA product code for BALLOON TEMP. PACING CATHETER?

The FDA product code for BALLOON TEMP. PACING 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 Ziehm International, 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.

View all 16 devices →

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

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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