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FDA 510(k)

LUMISCOPE MICRO 100

K-Number: K901726 · 1990-08-14

ApplicantLumiscope Co., Inc.
Decision Date1990-08-14
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LUMISCOPE MICRO 100 is the device name listed in this FDA 510(k) record. The listed applicant is Lumiscope Co., Inc.. It received FDA 510(k) clearance on 1990-08-14 under 510(k) number K901726. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMISCOPE MICRO 100?

LUMISCOPE MICRO 100 is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is Lumiscope Co., Inc.. The 510(k) number is K901726.

When did LUMISCOPE MICRO 100 receive FDA 510(k) clearance?

LUMISCOPE MICRO 100 received FDA 510(k) clearance on 1990-08-14, under 510(k) number K901726.

Who is the listed applicant for LUMISCOPE MICRO 100?

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

What is the FDA product code for LUMISCOPE MICRO 100?

The FDA product code for LUMISCOPE MICRO 100 is GZJ.

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Other records listing Lumiscope Co., 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: GZJ)

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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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