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FDA 510(k)

ELECTRO-TOUCH (ET) GLOVE

K-Number: K890981 · 1989-10-19

ApplicantPsychoenergetic Systems, Inc.
Decision Date1989-10-19
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-TOUCH (ET) GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Psychoenergetic Systems, Inc.. It received FDA 510(k) clearance on 1989-10-19 under 510(k) number K890981. 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 ELECTRO-TOUCH (ET) GLOVE?

ELECTRO-TOUCH (ET) GLOVE is a medical device that received FDA 510(k) clearance on 1989-10-19. The listed applicant is Psychoenergetic Systems, Inc.. The 510(k) number is K890981.

When did ELECTRO-TOUCH (ET) GLOVE receive FDA 510(k) clearance?

ELECTRO-TOUCH (ET) GLOVE received FDA 510(k) clearance on 1989-10-19, under 510(k) number K890981.

Who is the listed applicant for ELECTRO-TOUCH (ET) GLOVE?

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

What is the FDA product code for ELECTRO-TOUCH (ET) GLOVE?

The FDA product code for ELECTRO-TOUCH (ET) GLOVE is GXY.

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Other records listing Psychoenergetic Systems, Inc. as applicant

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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Related Devices (Code: GXY)

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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