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FDA 510(k)

LAMINARIA

K-Number: K955072 · 1996-05-22

Decision Date1996-05-22
Product CodeHDY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAMINARIA is the device name listed in this FDA 510(k) record. The listed applicant is Cti Corp., Ltd.. It received FDA 510(k) clearance on 1996-05-22 under 510(k) number K955072. The device is classified under product code HDY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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

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