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FDA 510(k)

OSCILLATING KNIFE AND ACCESSORIES

K-Number: K781412 · 1978-10-11

ApplicantCodman & Shurtleff, Inc.
Decision Date1978-10-11
Product CodeHMY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OSCILLATING KNIFE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1978-10-11 under 510(k) number K781412. The device is classified under product code HMY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSCILLATING KNIFE AND ACCESSORIES?

OSCILLATING KNIFE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1978-10-11. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K781412.

When did OSCILLATING KNIFE AND ACCESSORIES receive FDA 510(k) clearance?

OSCILLATING KNIFE AND ACCESSORIES received FDA 510(k) clearance on 1978-10-11, under 510(k) number K781412.

Who is the listed applicant for OSCILLATING KNIFE AND ACCESSORIES?

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

What is the FDA product code for OSCILLATING KNIFE AND ACCESSORIES?

The FDA product code for OSCILLATING KNIFE AND ACCESSORIES is HMY.

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Related Devices (Code: HMY)

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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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