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FDA 510(k)

ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM

K-Number: K892114 · 1989-10-13

ApplicantEclosion, Inc.
Decision Date1989-10-13
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Eclosion, Inc.. It received FDA 510(k) clearance on 1989-10-13 under 510(k) number K892114. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM?

ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Eclosion, Inc.. The 510(k) number is K892114.

When did ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM receive FDA 510(k) clearance?

ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM received FDA 510(k) clearance on 1989-10-13, under 510(k) number K892114.

Who is the listed applicant for ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM?

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

What is the FDA product code for ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM?

The FDA product code for ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM is HCC.

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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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