FDA 510(k)

SURGICAL OSCILLATING SAW

K-Number: K760958 · 1976-11-16

ApplicantAmerican Safety Equipment Corp.

Decision Date1976-11-16

Product CodeDZH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

SURGICAL OSCILLATING SAW is the device name listed in this FDA 510(k) record. The listed applicant is American Safety Equipment Corp.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760958. The device is classified under product code DZH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL OSCILLATING SAW?

SURGICAL OSCILLATING SAW is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is American Safety Equipment Corp.. The 510(k) number is K760958.

When did SURGICAL OSCILLATING SAW receive FDA 510(k) clearance?

SURGICAL OSCILLATING SAW received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760958.

Who is the listed applicant for SURGICAL OSCILLATING SAW?

The FDA 510(k) record lists American Safety Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL OSCILLATING SAW?

The FDA product code for SURGICAL OSCILLATING SAW is DZH.

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Other records listing American Safety Equipment Corp. as applicant

K801010KIRSCHNER WIRE K771699CARA-STAIN MODEL 3000 K760960SURGICAL WIRE DRIVER K760956SURGICAL MICRO DRILL K760959SURGICAL CHISEL K760957SURGICAL RECIPROCATING SAW

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Related Devices (Code: DZH)

K031793DENTATUS OSCIOMATDentatus USA , Ltd.K935443ADD LINE DEVICES(PARTS) ELECTRIC HANDPIECE SYSTEMSOsada Electric Co., Ltd.K760957SURGICAL RECIPROCATING SAWAmerican Safety Equipment Corp.

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.