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FDA 510(k)

MODEL 1240, SMALL E NET

K-Number: K960885 · 1996-04-26

ApplicantPhysiometrix, Inc.
Decision Date1996-04-26
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 1240, SMALL E NET is the device name listed in this FDA 510(k) record. The listed applicant is Physiometrix, Inc.. It received FDA 510(k) clearance on 1996-04-26 under 510(k) number K960885. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1240, SMALL E NET?

MODEL 1240, SMALL E NET is a medical device that received FDA 510(k) clearance on 1996-04-26. The listed applicant is Physiometrix, Inc.. The 510(k) number is K960885.

When did MODEL 1240, SMALL E NET receive FDA 510(k) clearance?

MODEL 1240, SMALL E NET received FDA 510(k) clearance on 1996-04-26, under 510(k) number K960885.

Who is the listed applicant for MODEL 1240, SMALL E NET?

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

What is the FDA product code for MODEL 1240, SMALL E NET?

The FDA product code for MODEL 1240, SMALL E NET is GXY.

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Other records listing Physiometrix, Inc. as applicant

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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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