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FDA 510(k)

MICROTOOLS

K-Number: K991104 · 1999-07-19

ApplicantConception Technology, Inc.
Decision Date1999-07-19
Product CodeMQH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MICROTOOLS is the device name listed in this FDA 510(k) record. The listed applicant is Conception Technology, Inc.. It received FDA 510(k) clearance on 1999-07-19 under 510(k) number K991104. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTOOLS?

MICROTOOLS is a medical device that received FDA 510(k) clearance on 1999-07-19. The listed applicant is Conception Technology, Inc.. The 510(k) number is K991104.

When did MICROTOOLS receive FDA 510(k) clearance?

MICROTOOLS received FDA 510(k) clearance on 1999-07-19, under 510(k) number K991104.

Who is the listed applicant for MICROTOOLS?

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

What is the FDA product code for MICROTOOLS?

The FDA product code for MICROTOOLS is MQH.

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Other records listing Conception Technology, 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: MQH)

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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