LAMINARIA
K-Number: K955072 · 1996-05-22
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Device Summary
Frequently Asked Questions
What is the LAMINARIA?
LAMINARIA is a medical device that received FDA 510(k) clearance on 1996-05-22. The listed applicant is Cti Corp., Ltd.. The 510(k) number is K955072.
When did LAMINARIA receive FDA 510(k) clearance?
LAMINARIA received FDA 510(k) clearance on 1996-05-22, under 510(k) number K955072.
Who is the listed applicant for LAMINARIA?
The FDA 510(k) record lists Cti Corp., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAMINARIA?
The FDA product code for LAMINARIA is HDY.
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.
Related Devices (Code: HDY)
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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