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FDA 510(k)

M170 PNEUMATICALLY OPERATED OSCILLATING SAW

K-Number: K914845 · 1992-01-13

ApplicantDesutter Medical , Ltd.
Decision Date1992-01-13
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

M170 PNEUMATICALLY OPERATED OSCILLATING SAW is the device name listed in this FDA 510(k) record. The listed applicant is Desutter Medical , Ltd.. It received FDA 510(k) clearance on 1992-01-13 under 510(k) number K914845. 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 M170 PNEUMATICALLY OPERATED OSCILLATING SAW?

M170 PNEUMATICALLY OPERATED OSCILLATING SAW is a medical device that received FDA 510(k) clearance on 1992-01-13. The listed applicant is Desutter Medical , Ltd.. The 510(k) number is K914845.

When did M170 PNEUMATICALLY OPERATED OSCILLATING SAW receive FDA 510(k) clearance?

M170 PNEUMATICALLY OPERATED OSCILLATING SAW received FDA 510(k) clearance on 1992-01-13, under 510(k) number K914845.

Who is the listed applicant for M170 PNEUMATICALLY OPERATED OSCILLATING SAW?

The FDA 510(k) record lists Desutter Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M170 PNEUMATICALLY OPERATED OSCILLATING SAW?

The FDA product code for M170 PNEUMATICALLY OPERATED OSCILLATING SAW is HSZ.

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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.

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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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