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FDA 510(k)

LD-I 75 AND LD-I 200

K-Number: K072551 · 2008-04-02

ApplicantMeditech International, Inc.
Decision Date2008-04-02
Product CodeNHN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LD-I 75 AND LD-I 200 is the device name listed in this FDA 510(k) record. The listed applicant is Meditech International, Inc.. It received FDA 510(k) clearance on 2008-04-02 under 510(k) number K072551. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LD-I 75 AND LD-I 200?

LD-I 75 AND LD-I 200 is a medical device that received FDA 510(k) clearance on 2008-04-02. The listed applicant is Meditech International, Inc.. The 510(k) number is K072551.

When did LD-I 75 AND LD-I 200 receive FDA 510(k) clearance?

LD-I 75 AND LD-I 200 received FDA 510(k) clearance on 2008-04-02, under 510(k) number K072551.

Who is the listed applicant for LD-I 75 AND LD-I 200?

The FDA 510(k) record lists Meditech International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LD-I 75 AND LD-I 200?

The FDA product code for LD-I 75 AND LD-I 200 is NHN.

Other records listing Meditech International, 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.

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Related Devices (Code: NHN)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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