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FDA 510(k)

COMPRESSAR UNIVERSAL (TM) SYSTEM

K-Number: K925809 · 1993-02-22

ApplicantInstromedix, Inc.
Decision Date1993-02-22
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COMPRESSAR UNIVERSAL (TM) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Instromedix, Inc.. It received FDA 510(k) clearance on 1993-02-22 under 510(k) number K925809. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSAR UNIVERSAL (TM) SYSTEM?

COMPRESSAR UNIVERSAL (TM) SYSTEM is a medical device that received FDA 510(k) clearance on 1993-02-22. The listed applicant is Instromedix, Inc.. The 510(k) number is K925809.

When did COMPRESSAR UNIVERSAL (TM) SYSTEM receive FDA 510(k) clearance?

COMPRESSAR UNIVERSAL (TM) SYSTEM received FDA 510(k) clearance on 1993-02-22, under 510(k) number K925809.

Who is the listed applicant for COMPRESSAR UNIVERSAL (TM) SYSTEM?

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

What is the FDA product code for COMPRESSAR UNIVERSAL (TM) SYSTEM?

The FDA product code for COMPRESSAR UNIVERSAL (TM) SYSTEM is DXC.

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Other records listing Instromedix, Inc. as applicant

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Related Devices (Code: DXC)

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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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