Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NUMED BALLOON PACING CATHETER

K-Number: K851246 · 1985-04-19

ApplicantNuMED, Inc.
Decision Date1985-04-19
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUMED BALLOON PACING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 1985-04-19 under 510(k) number K851246. 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 NUMED BALLOON PACING CATHETER?

NUMED BALLOON PACING CATHETER is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is NuMED, Inc.. The 510(k) number is K851246.

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

NUMED BALLOON PACING CATHETER received FDA 510(k) clearance on 1985-04-19, under 510(k) number K851246.

Who is the listed applicant for NUMED BALLOON PACING CATHETER?

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

What is the FDA product code for NUMED BALLOON PACING CATHETER?

The FDA product code for NUMED BALLOON 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 NuMED, 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 48 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.

↑