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FDA 510(k)

PRO-TORQ

K-Number: K000120 · 2000-02-03

ApplicantMicro Motors, Inc.
Decision Date2000-02-03
Product CodeEBW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRO-TORQ is the device name listed in this FDA 510(k) record. The listed applicant is Micro Motors, Inc.. It received FDA 510(k) clearance on 2000-02-03 under 510(k) number K000120. The device is classified under product code EBW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TORQ?

PRO-TORQ is a medical device that received FDA 510(k) clearance on 2000-02-03. The listed applicant is Micro Motors, Inc.. The 510(k) number is K000120.

When did PRO-TORQ receive FDA 510(k) clearance?

PRO-TORQ received FDA 510(k) clearance on 2000-02-03, under 510(k) number K000120.

Who is the listed applicant for PRO-TORQ?

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

What is the FDA product code for PRO-TORQ?

The FDA product code for PRO-TORQ is EBW.

Other records listing Micro Motors, Inc. as applicant

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Related Devices (Code: EBW)

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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