GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY
K-Number: K903840 · 1990-10-16
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Device Summary
Frequently Asked Questions
What is the GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY?
GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY is a medical device that received FDA 510(k) clearance on 1990-10-16. The listed applicant is Intec Medical, Inc.. The 510(k) number is K903840.
When did GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY receive FDA 510(k) clearance?
GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY received FDA 510(k) clearance on 1990-10-16, under 510(k) number K903840.
Who is the listed applicant for GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY?
The FDA 510(k) record lists Intec Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY?
The FDA product code for GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY is DYB.
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 Intec Medical, 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: DYB)
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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