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FDA 510(k)

MICRO-AIRE MODEL NUMBER: MK-426

K-Number: K905097 · 1990-12-21

Decision Date1990-12-21
Product CodeHBE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRO-AIRE MODEL NUMBER: MK-426 is the device name listed in this FDA 510(k) record. The listed applicant is Micro Surgical Instruments Corp.. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K905097. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-AIRE MODEL NUMBER: MK-426?

MICRO-AIRE MODEL NUMBER: MK-426 is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K905097.

When did MICRO-AIRE MODEL NUMBER: MK-426 receive FDA 510(k) clearance?

MICRO-AIRE MODEL NUMBER: MK-426 received FDA 510(k) clearance on 1990-12-21, under 510(k) number K905097.

Who is the listed applicant for MICRO-AIRE MODEL NUMBER: MK-426?

The FDA 510(k) record lists Micro Surgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-AIRE MODEL NUMBER: MK-426?

The FDA product code for MICRO-AIRE MODEL NUMBER: MK-426 is HBE.

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.

Other records listing Micro Surgical Instruments Corp. 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.

View all 15 devices →

Related Devices (Code: HBE)

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

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