NUMED BALLOON PACING CATHETER
K-Number: K843290 · 1985-01-14
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Device Summary
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 1985-01-14. The listed applicant is NuMED, Inc.. The 510(k) number is K843290.
When did NUMED BALLOON PACING CATHETER receive FDA 510(k) clearance?
NUMED BALLOON PACING CATHETER received FDA 510(k) clearance on 1985-01-14, under 510(k) number K843290.
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.
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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