CARDICARE MODEL MT-301F & MT-301C
K-Number: K032714 · 2003-10-22
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Device Summary
Frequently Asked Questions
What is the CARDICARE MODEL MT-301F & MT-301C?
CARDICARE MODEL MT-301F & MT-301C is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Lumiscope Co., Inc.. The 510(k) number is K032714.
When did CARDICARE MODEL MT-301F & MT-301C receive FDA 510(k) clearance?
CARDICARE MODEL MT-301F & MT-301C received FDA 510(k) clearance on 2003-10-22, under 510(k) number K032714.
Who is the listed applicant for CARDICARE MODEL MT-301F & MT-301C?
The FDA 510(k) record lists Lumiscope Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARDICARE MODEL MT-301F & MT-301C?
The FDA product code for CARDICARE MODEL MT-301F & MT-301C is FLL.
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 Lumiscope Co., 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: FLL)
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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