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FDA 510(k)

OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305

K-Number: K903650 · 1990-09-14

Decision Date1990-09-14
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305 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 1990-09-14 under 510(k) number K903650. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305?

OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305 is a medical device that received FDA 510(k) clearance on 1990-09-14. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K903650.

When did OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305 receive FDA 510(k) clearance?

OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305 received FDA 510(k) clearance on 1990-09-14, under 510(k) number K903650.

Who is the listed applicant for OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305?

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 OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305?

The FDA product code for OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305 is HWE.

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: HWE)

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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