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FDA 510(k)

ECHO-COM FOR MS-WINDOWS VERSION 2.0

K-Number: K960665 · 1996-05-07

ApplicantCone Instruments, Inc.
Decision Date1996-05-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHO-COM FOR MS-WINDOWS VERSION 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Cone Instruments, Inc.. It received FDA 510(k) clearance on 1996-05-07 under 510(k) number K960665. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHO-COM FOR MS-WINDOWS VERSION 2.0?

ECHO-COM FOR MS-WINDOWS VERSION 2.0 is a medical device that received FDA 510(k) clearance on 1996-05-07. The listed applicant is Cone Instruments, Inc.. The 510(k) number is K960665.

When did ECHO-COM FOR MS-WINDOWS VERSION 2.0 receive FDA 510(k) clearance?

ECHO-COM FOR MS-WINDOWS VERSION 2.0 received FDA 510(k) clearance on 1996-05-07, under 510(k) number K960665.

Who is the listed applicant for ECHO-COM FOR MS-WINDOWS VERSION 2.0?

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

What is the FDA product code for ECHO-COM FOR MS-WINDOWS VERSION 2.0?

The FDA product code for ECHO-COM FOR MS-WINDOWS VERSION 2.0 is LLZ.

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Official Source

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