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FDA 510(k)

MHS MED LIGHT 1000

K-Number: K021956 · 2002-08-13

ApplicantMicro Health Systems, Inc.
Decision Date2002-08-13
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MHS MED LIGHT 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Micro Health Systems, Inc.. It received FDA 510(k) clearance on 2002-08-13 under 510(k) number K021956. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MHS MED LIGHT 1000?

MHS MED LIGHT 1000 is a medical device that received FDA 510(k) clearance on 2002-08-13. The listed applicant is Micro Health Systems, Inc.. The 510(k) number is K021956.

When did MHS MED LIGHT 1000 receive FDA 510(k) clearance?

MHS MED LIGHT 1000 received FDA 510(k) clearance on 2002-08-13, under 510(k) number K021956.

Who is the listed applicant for MHS MED LIGHT 1000?

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

What is the FDA product code for MHS MED LIGHT 1000?

The FDA product code for MHS MED LIGHT 1000 is ILY.

Related Clinical Trials

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Other records listing Micro Health Systems, 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.

K030018MHS 7000K011981MHS 5000

Related Devices (Code: ILY)

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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