MODEL DMC-75 MINI-CATHETER SET
K-Number: K874307 · 1988-01-29
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Device Summary
Frequently Asked Questions
What is the MODEL DMC-75 MINI-CATHETER SET?
MODEL DMC-75 MINI-CATHETER SET is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K874307.
When did MODEL DMC-75 MINI-CATHETER SET receive FDA 510(k) clearance?
MODEL DMC-75 MINI-CATHETER SET received FDA 510(k) clearance on 1988-01-29, under 510(k) number K874307.
Who is the listed applicant for MODEL DMC-75 MINI-CATHETER SET?
The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL DMC-75 MINI-CATHETER SET?
The FDA product code for MODEL DMC-75 MINI-CATHETER SET is FPA.
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 Life-Tech Intl., 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: FPA)
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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