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FDA 510(k)

ESCAPE CONTROL MODULE

K-Number: K021995 · 2002-08-01

ApplicantSpecialty Drives Technologies, Inc.
Decision Date2002-08-01
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ESCAPE CONTROL MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Drives Technologies, Inc.. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K021995. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESCAPE CONTROL MODULE?

ESCAPE CONTROL MODULE is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Specialty Drives Technologies, Inc.. The 510(k) number is K021995.

When did ESCAPE CONTROL MODULE receive FDA 510(k) clearance?

ESCAPE CONTROL MODULE received FDA 510(k) clearance on 2002-08-01, under 510(k) number K021995.

Who is the listed applicant for ESCAPE CONTROL MODULE?

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

What is the FDA product code for ESCAPE CONTROL MODULE?

The FDA product code for ESCAPE CONTROL MODULE is ITI.

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Related Devices (Code: ITI)

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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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