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FDA 510(k)

MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER

K-Number: K851443 · 1985-05-03

Decision Date1985-05-03
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Aire Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1985-05-03 under 510(k) number K851443. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER?

MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER is a medical device that received FDA 510(k) clearance on 1985-05-03. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K851443.

When did MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER receive FDA 510(k) clearance?

MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER received FDA 510(k) clearance on 1985-05-03, under 510(k) number K851443.

Who is the listed applicant for MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER?

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

What is the FDA product code for MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER?

The FDA product code for MICRO-AIRE OSCILLATING SAW, 1740-000 & WIRE DRIVER is HSZ.

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-Aire Surgical Instruments, 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.

View all 40 devices →

Related Devices (Code: HSZ)

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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