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FDA 510(k)

EAST WEST INSTRUMENTS

K-Number: K941193 · 1994-11-09

ApplicantEast West Instruments, Inc.
Decision Date1994-11-09
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EAST WEST INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is East West Instruments, Inc.. It received FDA 510(k) clearance on 1994-11-09 under 510(k) number K941193. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAST WEST INSTRUMENTS?

EAST WEST INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-11-09. The listed applicant is East West Instruments, Inc.. The 510(k) number is K941193.

When did EAST WEST INSTRUMENTS receive FDA 510(k) clearance?

EAST WEST INSTRUMENTS received FDA 510(k) clearance on 1994-11-09, under 510(k) number K941193.

Who is the listed applicant for EAST WEST INSTRUMENTS?

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

What is the FDA product code for EAST WEST INSTRUMENTS?

The FDA product code for EAST WEST INSTRUMENTS is MDM.

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Related Devices (Code: MDM)

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

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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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